510(k) Report

FDA applicant

Gics Pharmaceuticals

Mchenry, IL4 decisions1980–19810 recalls

FDA records 4 decisions for Gics Pharmaceuticals (Mchenry, IL) from 1980 to 1981: 4 510(k) clearances. Most are in product codes DRS (Transducer, Blood-Pressure, Extravascular) and DTN (Reservoir, Blood, Cardiopulmonary Bypass). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Gics Pharmaceuticals since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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