tion procedures in subpart E of part 807 of this chapter. [47 FR 31142, July 16, 1982, as amended at 61 FR 1120, Jan. 16, 1996] 8868.5795 Tracheal tube cleaning brush. (a) Identification. A tracheal tube cleaning brush is a device consisting of a brush with plastic bristles intended to clean tracheal cannula devices after their removal from patients. (b) Classification. Class I. The device is exempt from the premarket notification procedures in Subpart E of Part 807. If the device is not labeled or otherwise represented as sterile, it is exempt from the current good manufacturing practice regulations in Part 820, with the exception of § 820.180, with respect to general requirements concerning records, and §820.198, with respect to complaint files. [51 FR 40388, Nov. 6, 1986] § 868.5800 Tracheostomy tube and tube cuff. (a) Identification. A tracheostomy tube and tube cuff is a device intended to be placed into a surgical opening of the trachea to facilitate ventilation to the lungs. The cuff may be a separate or integral part of the tracheostomy tube and is, when inflated, intended to establish a seal between the tracheal wall and the tracheostomy tube. The cuff is used to prevent the patient's aspiration of substances, such as blood or vomit, or to provide a means for positive-pressure ventilation of the patient. This device is made of either stainless steel or plastic. (b) Classification. Class II. [51 FR 40389, Nov. 6, 1986] § 868.5810 Airway connector. (a) Identification. An airway connector is a device intended to connect a breathing gas source to a tracheal tube, tracheostomy tube, or mask. (b) Classification. Class I. The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter. [47 FR 31142, July 16, 1982, as amended at 61 FR 1120, Jan. 16, 1996] § 868.5820 Dental protector. (a) Identification. A dental protector is a device intended to protect a patient's teeth during manipulative procedures within a patient's oral cavity. (b) Classification. Class I. The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter. [47 FR 31142, July 16, 1982, as amended at 61 FR 1120, Jan. 16, 1996] §868.5830 Autotransfusion apparatus. (a) Identification. An autotransfusion apparatus is a device used to collect and reinfuse the blood lost by a patient due to surgery or trauma. (b) Classification. Class II (performance standards). § 868.5860 Pressure tubing and acces sories. (a) Identification. Pressure tubing and accessories are flexible or rigid devices intended to deliver pressurized medical gases. (b) Classification. Class I. The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter. [47 FR 31142, July 16, 1982, as amended at 61 FR 1120, Jan. 16, 1996] § 868.5870 Nonrebreathing valve. (a) Identification. A nonrebreathing valve is a one-way valve that directs breathing gas flow to the patient and vents exhaled gases into the atmosphere. (b) Classification. Class II (performance standards). § 868.5880 Anesthetic vaporizer. (a) Identification. An anesthetic vaporizer is a device used to vaporize liquid anesthetic and deliver a controlled amount of the vapor to the patient. (b) Classification. Class II (performance standards). $868.5895 Continuous ventilator. (a) Identification. A continuous ventilator (respirator) is a device intended to mechanically control or assist patient breathing by delivering a predetermined percentage of oxygen in the breathing gas. Adult, pediatric, and (a) Identification. A cardiopulmonary emergency cart is a device intended to store and transport resuscitation supplies for emergency treatment. The device does not include any equipment used in cardiopulmonary resuscitation. (b) Classification. Class I. The device is exempt from the premarket notification procedures in Subpart E of Part 807 of this chapter. The device is also exempt from the current good manufacturing practice regulations in Part 820 of this chapter, with the exception of §820.180, with respect to general requirements concerning records, and § 820.198, with respect to complaint files. [47 FR 31142, July 16, 1982, as amended at 54 FR 25048, June 12, 1989] §868.6225 Nose clip. (a) Identification. A nose clip is a device intended to close a patient's external nares (nostrils) during diagnostic or therapeutic procedures. (b) Classification. Class I. The device is exempt from the premarket notification procedures in Subpart E of Part 807 of this chapter. The device is also exempt from the current good manufacturing practice regulations in Part 820 of this chapter, with the exception of §820.180, with respect to general requirements concerning records, and § 820.198, with respect to complaint files. [47 FR 31142, July 16, 1982, as amended at 54 FR 25048, June 12, 1989] § 868.6250 Portable air compressor. (a) Identification. A portable air compressor is a device intended to provide compressed air for medical purposes, e.g., to drive ventilators and other respiratory devices. (b) Classification. Class II (performance standards). 8868.6400 Calibration gas. (a) Identification. A calibration gas is a device consisting of a container of Subpart B-Cardiovascular Diagnostic 870.1025 Arrhythmia detector and alarm. 870.1130 Noninvasive blood pressure measurement system. 870.1140 Venous blood pressure manometer. 870.1230 Fiberoptic oximeter catheter. 870.1270 Intracavitary phonocatheter system. 870.1280 Steerable catheter. 870.1290 Steerable catheter control system. 870.1300 Catheter cannula. 870.1310 Vessel dilator for percutaneous catheterization. 870.1330 Catheter guide wire. 1870.1350 Catheter balloon repair kit. 870.1360 Trace microsphere. 870.1370 Catheter tip occluder. 870.1380 Catheter stylet. 870.1390 Trocar. 870.1425 Programmable puter. 870.1435 Single-function, preprogrammed di 870.3260 Vena cava clip. 167-072 0-96--10 (a) This part sets forth the classification of cardiovascular devices intended for human use that are in commercial distribution. (b) The identification of a device in a regulation in this part is not a precise description of every device that is, or will be, subject to the regulation. A manufacturer who submits a premarket notification submission for a device under Part 807 may not show merely that the device is accurately described by the section title and identification provisions of a regulation in this part, but shall state why the device is substantially equivalent to other devices, as required by §807.87. (c) To avoid duplicative listings, a cardiovascular device that has two or more types of uses (e.g., used both as a diagnostic device and as a therapeutic device) is listed only in one subpart. (d) References in this part to regulatory sections of the Code of Federal |