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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79. lappuse
... application does not meet the require- ments of §808.20 , he shall notify the State or political subdivision of the de- ficiencies in the application and of the opportunity to correct such defi- ciencies . A deficient application may be ...
... application does not meet the require- ments of §808.20 , he shall notify the State or political subdivision of the de- ficiencies in the application and of the opportunity to correct such defi- ciencies . A deficient application may be ...
103. lappuse
... Application and Administrative Action § 812.20 Application . ( a ) Submission . ( 1 ) A sponsor shall submit an application to FDA if the sponsor intends to use a significant risk device in an investigation , intends to conduct an ...
... Application and Administrative Action § 812.20 Application . ( a ) Submission . ( 1 ) A sponsor shall submit an application to FDA if the sponsor intends to use a significant risk device in an investigation , intends to conduct an ...
548. lappuse
... application for ap- proval as an accreditation body may be rejected . ( 3 ) FDA shall notify the applicant whether the application has been ap- proved or denied . That notification shall list any conditions associated with approval or ...
... application for ap- proval as an accreditation body may be rejected . ( 3 ) FDA shall notify the applicant whether the application has been ap- proved or denied . That notification shall list any conditions associated with approval or ...
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