# Ascep, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 9 (1979–1983): 9 510(k) clearances
- Product codes: FSM (4), KGX (2), HAO (1), GDX (1), EFQ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K830219: Various Instruments & Instrument Trays (Apr 12, 1983)
- K822893: G.E.V. Disposable Scalpels (Oct 22, 1982)
- K810004: Sterile Disposable Instrument Trays (Jan 26, 1981)
- K802726: Instruments Nonsterile & Sterile (Nov 19, 1980)
- K791886: I.V. Care Kit (Oct 26, 1979)
- K791885: I.V. Start Set (Oct 22, 1979)
- K791887: Central Venous Catheter Dressing Tray (Oct 17, 1979)
- K791888: Catheter Care Kit Reorder 7940&7941 (Oct 17, 1979)

Source page: https://510kreport.com/company/ascep