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. |
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156. lappuse
... patient's death , or the date the de- vice was returned to the distributor , permanently retired from use , or other- wise permanently disposed of . ( b ) A final distributor , upon sale or other distribution of a tracked device for use ...
... patient's death , or the date the de- vice was returned to the distributor , permanently retired from use , or other- wise permanently disposed of . ( b ) A final distributor , upon sale or other distribution of a tracked device for use ...
289. lappuse
... patient's airway resistance and lung volumes by measuring pres- sure changes while the patient is in an airtight box . ( b ) Classification . Class II ( perform- ance standards ) . $ 868.1760 Volume plethysmograph . ( a ) Identification ...
... patient's airway resistance and lung volumes by measuring pres- sure changes while the patient is in an airtight box . ( b ) Classification . Class II ( perform- ance standards ) . $ 868.1760 Volume plethysmograph . ( a ) Identification ...
407. lappuse
... Patient care reverse isola- tion chamber . ( a ) Identification . A patient care re- verse isolation chamber is a device consisting of a roomlike enclosure de- signed to prevent the entry of harmful airborne material . This device ...
... Patient care reverse isola- tion chamber . ( a ) Identification . A patient care re- verse isolation chamber is a device consisting of a roomlike enclosure de- signed to prevent the entry of harmful airborne material . This device ...
Saturs
1 For nomenclature changes to chapter I see 59 FR 14366 Mar 28 1994 | 3 |
Labeling | 13 |
Medical device reporting | 38 |
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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