# Surgipath

- Location (FDA's records): Mchenry, IL
- FDA decisions: 12 (1981–1982): 12 510(k) clearances
- Product codes: HZJ (3), HYJ (2), HYB (1), KEP (1), KDX (1), HZH (1), IFP (1), HYK (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
- K820027: Modified EA 50 (Feb 4, 1982)
- K812940: 10% Neutral Buffered Formalin Concent (Dec 10, 1981)
- K812087: EA 50 (Aug 13, 1981)
- K812086: EA 65 (Aug 13, 1981)
- K811826: Eosin Y (Jul 10, 1981)
- K811825: Orange G-6 (Jul 10, 1981)
- K810836: Decalcifier II (Apr 23, 1981)
- K810758: Gill's Hematoxylin #1 (Apr 14, 1981)

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