Medical Device Manufacturer · US , Mchenry , IL

Warner-Lambert Co. - FDA 510(k) Cleared Devices

50 submissions · 50 cleared · Since 1979

50

Total

50

Cleared

0

Denied

FDA 510(k) Regulatory Record - Warner-Lambert Co. Microbiology ✕

5 devices

1-5 of 5

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 Jul 23, 1985

GENERAL DIAGNOSTICS RAPID E. COLI TEST

Microbiology · 14d

Cleared May 01, 1985

GENERAL DIAGNOSTICS TICARCILLIN 75MCG SUSCEPT-DISK

Microbiology · 54d

Cleared Apr 24, 1985

GENERAL DIAGNOSTICS AUGMENTIN 30MCG SUSCEP DISK

Microbiology · 29d