Code of Federal Regulations 21 Parts 800 to 1299 Food and Drugs: Revised as of April 1 2006U.S. Government Printing Office, 2006 - 796 lappuses The Code of Federal Regulations is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the United States Federal Government. This volumwe contains the regulations about medical devices. |
No grāmatas satura
362. lappuse
... accessories . ( a ) Identification . An esophagoscope ( flexible or rigid ) and accessories is a tubular endoscopic device with any of a group of accessory devices which at- tach to the esophagoscope and is in- tended to examine or ...
... accessories . ( a ) Identification . An esophagoscope ( flexible or rigid ) and accessories is a tubular endoscopic device with any of a group of accessory devices which at- tach to the esophagoscope and is in- tended to examine or ...
365. lappuse
... accessories . 876.5130 Urological catheter and accessories . 876.5160 Urological clamp for males . 876.5210 Enema kit . 876.5220 Colonic irrigation system . 876.5250 Urine collector and accessories . 876.5270 Implanted electrical ...
... accessories . 876.5130 Urological catheter and accessories . 876.5160 Urological clamp for males . 876.5210 Enema kit . 876.5220 Colonic irrigation system . 876.5250 Urine collector and accessories . 876.5270 Implanted electrical ...
435. lappuse
... accessories . endoscopic cutter and accessories . 884.1100 884.1175 accessories . 884.1185 884.1300 Uterotubal carbon dioxide insufflator and accessories . 884.4160 Unipolar 884.1425 Perineometer . 884.1550 Amniotic fluid sampler ...
... accessories . endoscopic cutter and accessories . 884.1100 884.1175 accessories . 884.1185 884.1300 Uterotubal carbon dioxide insufflator and accessories . 884.4160 Unipolar 884.1425 Perineometer . 884.1550 Amniotic fluid sampler ...
Saturs
1 For nomenclature changes to chapter I see 59 FR 14366 Mar 28 1994 | 3 |
Labeling | 13 |
Medical device reporting | 38 |
39 citas sadaļas nav parādītas.
Citi izdevumi - Skatīt visu
Bieži izmantoti vārdi un frāzes
AC-powered accessories accreditation body amended at 65 ance standards application blood cardiopulmonary bypass catheter chapter subject Class II perform Class II special Classification clinical clude commercial distribution complaint files component current good manufacturing Date PMA dental denture device intended device is exempt device that consists disease electronic equipment facility FDA's fluoroscopic Food and Drug guidance document Identification image receptor immunological test system implanted intended for medical intended to measure July 25 labeling limitations mammography manufacturing practice manufacturing practice regula means medical purposes ment monitor notice of completion paragraph patient PDP is required plasma PMA or notice postmarket surveillance premarket approval premarket notification procedures procedures in subpart prosthesis radiation reagents regulation requirements concerning records respect to complaint Sept serological serum special controls specific submit subpart E surgical tion tissue trols type of device vice x-ray system