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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182. lappuse
... test system . 862.1115 Urinary bilirubin and its conjugates ( nonquantitative ) test system . 862.1117 B - type natriuretic peptide test sys- tem . 862.1118 Biotinidase test system . 862.1120 Blood gases ( Pco2Po2 ) and blood pH test ...
... test system . 862.1115 Urinary bilirubin and its conjugates ( nonquantitative ) test system . 862.1117 B - type natriuretic peptide test sys- tem . 862.1118 Biotinidase test system . 862.1120 Blood gases ( Pco2Po2 ) and blood pH test ...
183. lappuse
... test sys- tem . 862.1575 Phospholipid test system . 862.1580 Phosphorus ( inorganic ) test system . 862.1585 Human placental lactogen test sys- tem . 862.1590 Porphobilinogen test system . 862.1595 Porphyrins test system . 862.1600 ...
... test sys- tem . 862.1575 Phospholipid test system . 862.1580 Phosphorus ( inorganic ) test system . 862.1585 Human placental lactogen test sys- tem . 862.1590 Porphobilinogen test system . 862.1595 Porphyrins test system . 862.1600 ...
244. lappuse
... test system . inactivator 866.5270 C - reactive protein immunological test system . 866.5320 Properidin factor B immunological test system . 866.5330 Factor XIII , A , S , immunological test system . 866.5340 Ferritin immunological test ...
... test system . inactivator 866.5270 C - reactive protein immunological test system . 866.5320 Properidin factor B immunological test system . 866.5330 Factor XIII , A , S , immunological test system . 866.5340 Ferritin immunological test ...
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