# Surgipath Medical Industries, Inc.

- Location (FDA's records): Grayslake, IL
- FDA decisions: 30 (1977–1988): 30 510(k) clearances
- Product codes: IFP (4), KEO (3), HHT (3), KER (2), IDZ (2), IDL (2), IDO (1), KEP (1), KEM (1), LDZ (1), KDX (1), IFZ (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
- K883217: Schiff Reagent (Aug 5, 1988)
- K881921: C-E Brush (Jul 19, 1988)
- K881922: Cytojars Prefilled with Cytology Preservative (May 25, 1988)
- K881659: Tissue Section Adhesive (Apr 21, 1988)
- K863549: Reusable/Disposable Autopsy Knife Set (Sep 30, 1986)
- K863616: Knife Maker (Sep 25, 1986)
- K863548: Rotary Microtome (Sep 19, 1986)
- K863483: Cassette Embosseer (Sep 16, 1986)

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