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 75.
716. lappuse
... tissue , except as specified in this part . ( c ) Regulations in this chapter do not apply to autologous human tissue . ( d ) Regulations in this chapter do not apply to hospitals or other clinical fa- cilities that receive and store ...
... tissue , except as specified in this part . ( c ) Regulations in this chapter do not apply to autologous human tissue . ( d ) Regulations in this chapter do not apply to hospitals or other clinical fa- cilities that receive and store ...
718. lappuse
... tissue procured under legislative consent where a donor med- ical history screening interview has not occurred , a physical assessment of the donor is required and other avail- able information shall be reviewed . The corneal tissue ...
... tissue procured under legislative consent where a donor med- ical history screening interview has not occurred , a physical assessment of the donor is required and other avail- able information shall be reviewed . The corneal tissue ...
720. lappuse
... tissue will be handled in accord- ance with FDA's procedures on disclo- sure of information as set forth in 21 CFR part 20 of this chapter . § 1270.42 Human tissue offered for im- port . ( a ) When human tissue is offered for entry ...
... tissue will be handled in accord- ance with FDA's procedures on disclo- sure of information as set forth in 21 CFR part 20 of this chapter . § 1270.42 Human tissue offered for im- port . ( a ) When human tissue is offered for entry ...
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