FDA applicant
Gics Pharmaceuticals
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
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.
Planning a device like Gics Pharmaceuticals’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report