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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15. lappuse
... statements . ( a ) A word , statement , or other infor- mation required by or under authority of the act to appear on the label may lack that prominence and conspicuous- ness required by section 502 ( c ) of the act by reason , among ...
... statements . ( a ) A word , statement , or other infor- mation required by or under authority of the act to appear on the label may lack that prominence and conspicuous- ness required by section 502 ( c ) of the act by reason , among ...
28. lappuse
... statement that a hearing aid will not restore normal hearing and will not prevent or improve a hearing impairment resulting from organic conditions . ( ix ) A statement that in most cases infrequent use of a hearing aid does not permit ...
... statement that a hearing aid will not restore normal hearing and will not prevent or improve a hearing impairment resulting from organic conditions . ( ix ) A statement that in most cases infrequent use of a hearing aid does not permit ...
35. lappuse
... statement may be used : NOTE : The indented statement below is re- quired by the Federal government's Clean Air Act for all products containing or manu- factured with chlorofluorocarbons ( CFC's ) [ or name of other class I substance ...
... statement may be used : NOTE : The indented statement below is re- quired by the Federal government's Clean Air Act for all products containing or manu- factured with chlorofluorocarbons ( CFC's ) [ or name of other class I substance ...
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