FDA applicant

Fmc Corp.

Walker, MI2 decisions1985–19950 recalls

FDA records 2 decisions for Fmc Corp. (Walker, MI) from 1985 to 1995: 2 510(k) clearances. Most are in product codes JJN (Apparatus, Electrophoresis, For Clinical Use) and JZR (Support Gels). 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, clinical chemistry panel, where it files most

How often FDA has decided Fmc Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fmc Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Fmc Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Fmc Corp.

Which product codes does it file in?

What has FDA decided for it lately?