FDA applicant

M.C. Johnson Co., Inc.

Naples, FL3 decisions1983–19950 recalls

FDA records 3 decisions for M.C. Johnson Co., Inc. (Naples, FL) from 1983 to 1995: 3 510(k) clearances. Most are in product codes KNT (Tubes, Gastrointestinal (And Accessories)) and LDR (Controller, Infusion, Intravascular, Electronic). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for M.C. Johnson Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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M.C. Johnson Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?