# Op-Co Medical Products, Ltd.

- Location (FDA's records): New York City, NY
- FDA decisions: 3 (1991–1995): 3 510(k) clearances
- Product codes: KMK (3)
- 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
- K941098: Secure-Site (Aug 9, 1995)
- K932757: Securodrip (TM) I.V. Armboard (Dec 8, 1993)
- K912660: Securodrip (Dec 4, 1991)

Source page: https://510kreport.com/company/op-co-medical-products