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
218. lappuse
... device intended to measure gentamicin , an antibiotic drug , in human specimens . Measurements ob- tained by this device are used in the di- agnosis and treatment of gentamicin overdose and in monitoring levels of gentamicin to ensure ...
... device intended to measure gentamicin , an antibiotic drug , in human specimens . Measurements ob- tained by this device are used in the di- agnosis and treatment of gentamicin overdose and in monitoring levels of gentamicin to ensure ...
219. lappuse
... device intended to measure morphine , an addictive narcotic pain- relieving drug , and its analogs in serum , urine , and gastric contents . Measurements obtained by this device are used in the diagnosis and treat- ment of morphine use ...
... device intended to measure morphine , an addictive narcotic pain- relieving drug , and its analogs in serum , urine , and gastric contents . Measurements obtained by this device are used in the diagnosis and treat- ment of morphine use ...
288. lappuse
... device intended to measure the concentration of carbon monoxide in a gas mixture to aid in de- termining the patient's ventilatory status . The device may use techniques such as infrared absorption or gas chro- matography . ( b ) ...
... device intended to measure the concentration of carbon monoxide in a gas mixture to aid in de- termining the patient's ventilatory status . The device may use techniques such as infrared absorption or gas chro- matography . ( b ) ...
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