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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78. lappuse
... tion , shall be submitted to the Division of Dockets Management ( HFA - 305 ) , Food and Drug Administration , 5630 Fishers Lane , rm . 1061 , Rockville , MD 20852. The outside wrapper of any appli- cation , report , or correspondence ...
... tion , shall be submitted to the Division of Dockets Management ( HFA - 305 ) , Food and Drug Administration , 5630 Fishers Lane , rm . 1061 , Rockville , MD 20852. The outside wrapper of any appli- cation , report , or correspondence ...
79. lappuse
... tion either to grant or to deny an ex- emption from preemption . The Com- missioner shall also issue in the FED- ERAL REGISTER a notice of opportunity to request an oral hearing before the Commissioner or the Commissioner's designee ...
... tion either to grant or to deny an ex- emption from preemption . The Com- missioner shall also issue in the FED- ERAL REGISTER a notice of opportunity to request an oral hearing before the Commissioner or the Commissioner's designee ...
81. lappuse
... tion has exempted them from preemp- tion under section 521 ( b ) of the act : Ha- waii Revised Statutes , chapter 451A , §14.1 , subsection ( a ) with respect to medical examination of a child 10 years of age or under , and subsection ...
... tion has exempted them from preemp- tion under section 521 ( b ) of the act : Ha- waii Revised Statutes , chapter 451A , §14.1 , subsection ( a ) with respect to medical examination of a child 10 years of age or under , and subsection ...
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