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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193. lappuse
... amended at 65 FR 2306 , Jan. 14 , 2000 ] § 862.1250 Desoxycorticosterone system . ( a ) Identification . test A desoxycorticosterone test system is a device intended measure to desoxycorticosterone ( DOC ) in plasma and urine . DOC ...
... amended at 65 FR 2306 , Jan. 14 , 2000 ] § 862.1250 Desoxycorticosterone system . ( a ) Identification . test A desoxycorticosterone test system is a device intended measure to desoxycorticosterone ( DOC ) in plasma and urine . DOC ...
200. lappuse
Revised as of April 1 2006 Office of the Federal Register, Office of the Federal Register (U.S.) Staff. subpart E of part 807 of this chapter subject to § 862.9 . [ 52 FR 16122 , May 1 , 1987 , as amended at 65 FR 2307 , Jan. 14 , 2000 ] ...
Revised as of April 1 2006 Office of the Federal Register, Office of the Federal Register (U.S.) Staff. subpart E of part 807 of this chapter subject to § 862.9 . [ 52 FR 16122 , May 1 , 1987 , as amended at 65 FR 2307 , Jan. 14 , 2000 ] ...
204. lappuse
... amended at 65 FR 2308 , Jan. 14 , 2000 ] § 862.1610 Pregnanetriol test system . ( a ) Identification . A pregnanetriol test system is a device intended to measure pregnanetriol ( a precursor in the bio- synthesis of the adrenal hormone ...
... amended at 65 FR 2308 , Jan. 14 , 2000 ] § 862.1610 Pregnanetriol test system . ( a ) Identification . A pregnanetriol test system is a device intended to measure pregnanetriol ( a precursor in the bio- synthesis of the adrenal hormone ...
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