# Angiomed U.S., Inc.

- Location (FDA's records): Anaheim, CA
- FDA decisions: 24 (1986–1988): 24 510(k) clearances
- Product codes: GBO (5), KOD (4), FAD (2), GDM (1), FFL (1), GES (1), KOB (1), GCD (1), KGZ (1), GBZ (1), FGE (1), DWO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Cook, Inc.: 1 (https://510kreport.com/company/cook)

## Its most-cited devices
- K854909: Pediatric Percutaneous Nephrostomy Sets (1986), cited by 1

## Recent decisions
- K874771: Angiomed Introducing Sets (Jan 12, 1988)
- K874585: Angiomed Osty-Cut Bone Biopsy Needle (Dec 2, 1987)
- K864225: Angiomed Ureteral D&M Sets/Ureteroscopy Guid Stent (Jan 30, 1987)
- K863386: Vesico Suprapubic Bladder Drainage & Exchange Sets (Oct 24, 1986)
- K862805: Angiomed Vac-U-Cut Biopsy Needle (Sep 29, 1986)
- K863446: Angiomed High Pressure Connectors (Sep 23, 1986)
- K854910: Angioflow (Jul 17, 1986)
- K854912: Angiomed Guied Wires (Apr 16, 1986)

Source page: https://510kreport.com/company/angiomed-us