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
1.3. rezultāts no 83.
29. lappuse
... evaluation . The audiologist or hearing aid dispenser will conduct a hearing aid evaluation to as- sess your ability to hear with and without a hearing aid . The hearing aid evaluation will enable the audiologist or dispenser to select ...
... evaluation . The audiologist or hearing aid dispenser will conduct a hearing aid evaluation to as- sess your ability to hear with and without a hearing aid . The hearing aid evaluation will enable the audiologist or dispenser to select ...
30. lappuse
... evaluation must have taken place within the preceding 6 months . ( 2 ) Waiver to the medical evaluation re- quirements . If the prospective hearing aid user is 18 years of age or older , the hearing aid dispenser may afford the ...
... evaluation must have taken place within the preceding 6 months . ( 2 ) Waiver to the medical evaluation re- quirements . If the prospective hearing aid user is 18 years of age or older , the hearing aid dispenser may afford the ...
576. lappuse
... Evaluation . FDA shall evaluate annually the per- formance of each certification agency . The evaluation shall include the use of performance indicators that address the adequacy of program performance in certification , inspection ...
... Evaluation . FDA shall evaluate annually the per- formance of each certification agency . The evaluation shall include the use of performance indicators that address the adequacy of program performance in certification , inspection ...
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