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 65.
387. lappuse
... implantation . The device is intended to be implanted to augment or recon- struct the female breast . as and ( 2 ) Double - lumen silicone gel - filled breast prosthesis . A double lumen sili- cone gel - filled breast prosthesis is a ...
... implantation . The device is intended to be implanted to augment or recon- struct the female breast . as and ( 2 ) Double - lumen silicone gel - filled breast prosthesis . A double lumen sili- cone gel - filled breast prosthesis is a ...
432. lappuse
... implanted receiver with electrodes that are placed on the pa- tient's cerebellum and an external transmitter for transmitting the stim- ulating pulses across the patient's skin to the implanted receiver . ( b ) Classification . Class ...
... implanted receiver with electrodes that are placed on the pa- tient's cerebellum and an external transmitter for transmitting the stim- ulating pulses across the patient's skin to the implanted receiver . ( b ) Classification . Class ...
433. lappuse
... Implanted spinal cord stim- ulator for bladder evacuation . ( a ) Identification . An implanted spinal cord stimulator for bladder evacuation is an electrical stimulator used to empty the bladder of a paraplegic pa- tient who has a ...
... Implanted spinal cord stim- ulator for bladder evacuation . ( a ) Identification . An implanted spinal cord stimulator for bladder evacuation is an electrical stimulator used to empty the bladder of a paraplegic pa- tient who has a ...
Saturs
1 For nomenclature changes to chapter I see 59 FR 14366 Mar 28 1994 | 3 |
Labeling | 13 |
Medical device reporting | 38 |
39 citas sadaļas nav parādītas.
Citi izdevumi - Skatīt visu
Bieži izmantoti vārdi un frāzes
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