# Hospal Medical Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 55 (1977–1989): 55 510(k) clearances
- Product codes: KDI (20), FKQ (7), KOC (4), FJG (4), FIE (4), FJI (4), FKP (3), CBK (1), CAF (1), KDT (1), FII (1), FRN (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
- K893742: Filtral TM 20 Hemodialyzer/Filter (Jul 24, 1989)
- K884365: Multiflow (TM) 60 Kit (Dec 8, 1988)
- K884326: Filtral TM 8 Hemodialyzer (Dec 5, 1988)
- K883307: Cardioflow 100 Hemoconcentrator/Preparation Kit (Oct 12, 1988)
- K872767: Filtral 10, Filtral 12, Filtral 16 Hemodialyzer (Dec 29, 1987)
- K871218: Monitral S GS Hemodialysis Single Patient Unit (Apr 30, 1987)
- K863961: Hospal Biospal 1800S (Dec 17, 1986)
- K863592: Disscap 80E, 110E, 140E, 160E (Sep 25, 1986)

Source page: https://510kreport.com/company/hospal-medical