FDA applicant

C.B. Fleet Co., Inc.

Washington, DC2 decisions1982–19990 recalls

FDA records 2 decisions for C.B. Fleet Co., Inc. (Washington, DC) from 1982 to 1999: 2 510(k) clearances. Most are in product codes HIS (Condom) and KHE (Reagent, Occult Blood). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, obstetrics and gynecology panel, where it files most

How often FDA has decided C.B. Fleet Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for C.B. Fleet Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — C.B. Fleet Co., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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C.B. Fleet Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?