# Vomed Volzer Medizintechnik GmbH & Co.

- Location (FDA's records): Amsterdam, Nh, NL
- FDA decisions: 3 (2002–2002): 3 510(k) clearances
- Product codes: FGI (1), DRC (1), HIF (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
- K023019: Vomed Urethra Olive, Models 1420 000, 1425 000, 1430 000 (Dec 10, 2002)
- K022257: Vomed Peripheral Vascular Accessories, Models 1010 XXX-7090 XXX & 9006 XXX-9011 XXX (Oct 4, 2002)
- K022318: Vomed Endoscopic and Urological Accessories (Sep 19, 2002)

Source page: https://510kreport.com/company/vomed-volzer-medizintechnik