Warner-Lambert Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
50
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K024160NEOSPORIN SCAR SOLUTIONMarch 17, 2003
K893452EXTRA STRENGTH EFFERGRIP DENTURE ADHESIVE CREAMJune 22, 1989
K870584O.P.T.(TM) OVULATION PREDICTION TESTNovember 25, 1987
K861510MULTILUMEN VIAPIC CENTRAL LINE CATHETERJune 9, 1986
K852689GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISKAugust 19, 1985
K852967GENERAL DIAGNOSTICS' CEFTRIAXONE 30MCG SUSDEP DISKAugust 19, 1985
K852843GENERAL DIAGNOSTICS COAG-A-MATE XCAugust 13, 1985
K852889GENERAL DIAGNOSTICS RAPID E. COLI TESTJuly 23, 1985
K850412GEN. DIAG. CHROMOSTRATE ANTITHROMBIN III ASSAYMay 8, 1985
K850409GEN. DIAG. CHROMOSTRATE REF. PLASMAMay 8, 1985
K850410GEN. DIAG. CHROMOSTRATE PLASMINOGEN ASSAYMay 8, 1985
K850411GEN. DIAG. CHROMOSTRATE ALPHA-2 ANTIPLASMIN ASSAYMay 8, 1985
K850486GENERAL DIAG. CHROMOSTRATE HEPARIN ASSAYMay 8, 1985
K850957GENERAL DIAGNOSTICS TICARCILLIN 75MCG SUSCEPT-DISKMay 1, 1985
K851228GENERAL DIAGNOSTICS AUGMENTIN 30MCG SUSCEP DISKApril 24, 1985
K833369EARLY DETECTORAugust 2, 1984
K833093VANISH IIDecember 12, 1983
K833092DESERET ANGIO-GUIDE LARGE VEIN CATH.November 21, 1983
K833091DESERET SUBCLAVIAN JUGULAR CATH-SETNovember 21, 1983
K833352GEN. DIAGNOSTICS LOW FIBRINOGEN CONTROLNovember 3, 1983