FDA applicant

G.D. Searle and Co.

Mchenry, IL56 decisions1976–19820 recalls

FDA records 56 decisions for G.D. Searle and Co. (Mchenry, IL) from 1976 to 1982: 56 510(k) clearances. Most are in product codes IYO (System, Imaging, Pulsed Echo, Ultrasonic) and CDP (Radioimmunoassay, Total Triiodothyronine). 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 G.D. Searle and Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for G.D. Searle and Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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G.D. Searle and Co.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?