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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238. lappuse
... tube is a cast - iron tunnel extending from one post office to another , through which the mails are transported . Its location beneath the ground makes access to the mails during transit practically impossible . The tube terminals ...
... tube is a cast - iron tunnel extending from one post office to another , through which the mails are transported . Its location beneath the ground makes access to the mails during transit practically impossible . The tube terminals ...
477. lappuse
... tube Mail Service. Outgoing mail to be transported by tubes must be brought from the distributing cases to the point where the pneumatic tubes are located , there placed in the tube containers by post - office clerks , and the containers ...
... tube Mail Service. Outgoing mail to be transported by tubes must be brought from the distributing cases to the point where the pneumatic tubes are located , there placed in the tube containers by post - office clerks , and the containers ...
665. lappuse
... Tube ATR Tube Magnetron Trav.Wave Tube Dual Gas Switching Tube TR Tube Shutter & TR Tube TR Tube Klystron Kiystron Broad band device for shorting wave guide Magnetron ATR Tube Shutter & ТЕ Tube Shutter & TR Tube Shutter 86 TR Tube ...
... Tube ATR Tube Magnetron Trav.Wave Tube Dual Gas Switching Tube TR Tube Shutter & TR Tube TR Tube Klystron Kiystron Broad band device for shorting wave guide Magnetron ATR Tube Shutter & ТЕ Tube Shutter & TR Tube Shutter 86 TR Tube ...
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