# Angeion Corp.

- Location (FDA's records): Plymouth, MN
- FDA decisions: 7 (1987–1993): 7 510(k) clearances
- Product codes: DYB (3), MAV (1), DXT (1), ODC (1), GBX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- B.Braun Medical, Inc.: 4 (https://510kreport.com/company/b-braun-medical)
- Medtronic Vascular: 3 (https://510kreport.com/company/medtronic-vascular)

## Its most-cited devices
- K894446: Angeion Hemostasis Valve Introducer (1989), cited by 3
- K895580: Y-Adapter W/Thouy Borst (1990), cited by 3
- K871153: Catheter Introducer (1987), cited by 1

## Recent decisions
- K921757: Angeion Igital Angeflator (Mar 18, 1993)
- K925533: Angestat (R) Pericardial Drainage Sheath Set (Jan 12, 1993)
- K915719: Angeion Endoscopic Valve Seal (Feb 18, 1992)
- K902377: Angeflator (TM) (Dec 13, 1990)
- K895580: Y-Adapter W/Thouy Borst (Apr 30, 1990)
- K894446: Angeion Hemostasis Valve Introducer (Nov 30, 1989)
- K871153: Catheter Introducer (Jun 24, 1987)

Source page: https://510kreport.com/company/angeion