FDA applicant
American Pharmaseal Div. Ahsc
FDA records 64 decisions for American Pharmaseal Div. Ahsc (Mchenry, IL) from 1980 to 1987: 64 510(k) clearances. Most are in product codes KOD (Catheter, Urological) and DQY (Catheter, Percutaneous). 2 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided American Pharmaseal Div. Ahsc’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for American Pharmaseal Div. Ahsc since 2007.
Recalls per year
1in 2026
Class I Class II/III not classified
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