# Euro-Med Intl.

- Location (FDA's records): Danville, CA
- FDA decisions: 16 (1985–1988): 16 510(k) clearances
- Product codes: KDC (7), FZS (2), FTY (1), KNW (1), PCF (1), HRX (1), EMF (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
- K883884: Prostatic Core-Cut Needle (Dec 5, 1988)
- K882404: Kevor-Curette (Jul 8, 1988)
- K854896: Hook Scissor (May 2, 1986)
- K854898: Atlantic Grasper (May 2, 1986)
- K854897: Max-I-Grasp (May 2, 1986)
- K854901: Pacific Grasper (May 2, 1986)
- K854890: Hook Probe (May 2, 1986)
- K854895: Basket Forcep (May 2, 1986)

Source page: https://510kreport.com/company/euro-med-intl