# Warner-Lambert Co.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 51 (1979–2003): 50 510(k) clearances and 1 original PMA approval
- Product codes: FOZ (8), JTN (4), JJY (3), KGO (2), KGZ (2), FCR (2), JHJ (2), NAD (1), KTZ (1), FWY (1), LGP (1), JBQ (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Bio Med Sciences, Inc.: 2 (https://510kreport.com/company/bio-med-sciences)

## Recent decisions
- K024160: Neosporin Scar Solution (Mar 17, 2003)
- K893452: Extra Strength Effergrip Denture Adhesive Cream (Jun 22, 1989)
- K870584: O.P.T.(TM) Ovulation Prediction Test (Nov 25, 1987)
- K861510: Multilumen Viapic Central Line Catheter (Jun 9, 1986)
- K852689: General Diagnostics Ceftazidime 30 MCG Susc Disk (Aug 19, 1985)
- K852967: General Diagnostics' Ceftriaxone 30MCG Susdep Disk (Aug 19, 1985)
- K852843: General Diagnostics Coag-a-Mate XC (Aug 13, 1985)
- K852889: General Diagnostics Rapid E. Coli Test (Jul 23, 1985)

Source page: https://510kreport.com/company/warner-lambert