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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350. lappuse
... unit . ( a ) Identification . An oral irrigation unit is an AC - powered device intended to provide a pressurized stream of water to remove food particles from be- tween the teeth and promote good peri- odontal ( gum ) condition . ( b ) ...
... unit . ( a ) Identification . An oral irrigation unit is an AC - powered device intended to provide a pressurized stream of water to remove food particles from be- tween the teeth and promote good peri- odontal ( gum ) condition . ( b ) ...
560. lappuse
... units . No more than one sur- vey of a specific unit within a period of 60 days can be counted towards the total mammography unit survey re- quirement . After April 28 , 1999 , experi- ence conducting surveys must be ac- quired under ...
... units . No more than one sur- vey of a specific unit within a period of 60 days can be counted towards the total mammography unit survey re- quirement . After April 28 , 1999 , experi- ence conducting surveys must be ac- quired under ...
568. lappuse
... units or image processors shall be conducted whenever a new unit or processor is installed , a unit or proc essor is disassembled and reassembled at the same or a new location , or major components of a mammography unit or processor ...
... units or image processors shall be conducted whenever a new unit or processor is installed , a unit or proc essor is disassembled and reassembled at the same or a new location , or major components of a mammography unit or processor ...
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