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Parke-Davis Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
47
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K861725INTRACATH INTRAVENOUS CATHETER PLACEMENT UNITDecember 4, 1986
K862119DESERET FLO-THRU INJECTATE TEMPERATURE SENSORAugust 29, 1986
K855120ATI DISPOSABLE BIOLOGICAL TEST PACKJune 18, 1986
K860570ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICEMarch 31, 1986
K860290VIAPIC CENTRAL LINE CATHETERMarch 18, 1986
K852192DISPOSABLE STEAM BIOLOGICAL TEST PACKNovember 1, 1985
K841967DESERET THERMODILUTION CARDIAC OUTPUTAugust 19, 1985
K851327DESERET ARTERIAL CATHETERJune 14, 1985
K852078SPECTRUM(TENTATIVE)June 7, 1985
K844840DESERET INTRODUCER SETMay 16, 1985
K850505DESERET EPIDURAL CATHETER W/TOUGHY-BORST ADAPTERMarch 11, 1985
K850439DESERET EPIDURAL CATHETERMarch 5, 1985
K843033DESERET INTRAVASCULAR CATHETERDecember 3, 1984
K844113DESERET SUBCLAVIAN JUGULAR CATHETER SETNovember 28, 1984
K844219DESERET DENTRAL LINE CATHETERNovember 28, 1984
K841968DESERET DISPOSABLE PRESSURE TRANSDUCERAugust 6, 1984
K841317DESERET HEPARIN COATED FLOW DIRECTEDJune 11, 1984
K841251DESERET HEPARIN COATED FLOW CATHJune 11, 1984
K841168STERILIZATION PROCESS INDICATORMay 9, 1984
K840958DESERET LONG TERM INDWELLING CATHETERApril 17, 1984