# Snyder Laboratories, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 16 (1978–1984): 16 510(k) clearances
- Product codes: GCY (5), FCM (3), BYY (2), GBS (1), EYN (1), BSY (1), KNX (1), KDQ (1), BTA (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
- K843906: Snyder Hemovac Wound Drainage Devices (Nov 5, 1984)
- K821321: Snyder Debribement System LDP-1 (Aug 6, 1982)
- K800861: Snyder Hemovac Chest Drainage Solution (May 2, 1980)
- K800578: Surgivac TM (Apr 16, 1980)
- K800543: Snyder Hysterectomy Y Tube Kit (Apr 16, 1980)
- K800577: Snyder Hemovac TM Vented Wound Kit (Apr 16, 1980)
- K800542: 100 ML Snyder Hemovac (Apr 2, 1980)
- K790607: Greenline Irrigation Trays (May 11, 1979)

Source page: https://510kreport.com/company/snyder-laboratories