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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vi. lappuse
... material , like any other properly issued regulation , has the force of law . What is a proper incorporation by reference ? The Director of the Federal Register will approve an incorporation by reference only when the requirements of 1 ...
... material , like any other properly issued regulation , has the force of law . What is a proper incorporation by reference ? The Director of the Federal Register will approve an incorporation by reference only when the requirements of 1 ...
326. lappuse
... material . 872.3660 Impression material . 872.3661 Optical Impression Systems for CAD / CAM . 872.3670 Resin impression tray material . 872.3680 Polytetrafluoroethylene ( PTFE ) vitreous carbon materials . 872.3690 Tooth shade resin ...
... material . 872.3660 Impression material . 872.3661 Optical Impression Systems for CAD / CAM . 872.3670 Resin impression tray material . 872.3680 Polytetrafluoroethylene ( PTFE ) vitreous carbon materials . 872.3690 Tooth shade resin ...
339. lappuse
... material . ( a ) Identification . Impression material is a device composed of materials such as alginate or polysulfide intended to be placed on a preformed impression tray and used to reproduce the struc- ture of a patient's teeth and ...
... material . ( a ) Identification . Impression material is a device composed of materials such as alginate or polysulfide intended to be placed on a preformed impression tray and used to reproduce the struc- ture of a patient's teeth and ...
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