Warner-Lambert Co. - FDA 510(k) Cleared Devices
50
Total
50
Cleared
0
Denied
Warner-Lambert Co. has 50 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 50 cleared submissions from 1979 to 2003.
Browse the FDA 510(k) cleared devices submitted by Warner-Lambert Co. Filter by specialty or product code using the sidebar.
50 devices
Cleared
Mar 17, 2003
NEOSPORIN SCAR SOLUTION
General & Plastic Surgery
90d
Cleared
Jun 22, 1989
EXTRA STRENGTH EFFERGRIP DENTURE ADHESIVE CREAM
Radiology
50d
Cleared
Nov 25, 1987
O.P.T.(TM) OVULATION PREDICTION TEST
Chemistry
287d
Cleared
Jun 09, 1986
MULTILUMEN VIAPIC CENTRAL LINE CATHETER
General Hospital
47d
Cleared
Aug 19, 1985
GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK
Microbiology
55d
Cleared
Aug 19, 1985
GENERAL DIAGNOSTICS' CEFTRIAXONE 30MCG SUSDEP DISK
Microbiology
35d
Cleared
Aug 13, 1985
GENERAL DIAGNOSTICS COAG-A-MATE XC
Hematology
39d
Cleared
Jul 23, 1985
GENERAL DIAGNOSTICS RAPID E. COLI TEST
Microbiology
14d
Cleared
May 08, 1985
GEN. DIAG. CHROMOSTRATE REF. PLASMA
Hematology
93d
Cleared
May 08, 1985
GEN. DIAG. CHROMOSTRATE PLASMINOGEN ASSAY
Immunology
93d
Cleared
May 08, 1985
GEN. DIAG. CHROMOSTRATE ALPHA-2 ANTIPLASMIN ASSAY
Immunology
93d
Cleared
May 08, 1985
GEN. DIAG. CHROMOSTRATE ANTITHROMBIN III ASSAY
Hematology
93d
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