# Angiomedics, Inc.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 8 (1984–1987): 8 510(k) clearances
- Product codes: DQO (3), DYB (2), DWF (1), LIT (1), DXT (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
- K873195: Schneider-Shiley Angioport (TM) Ptca Intro W/Hemo (Dec 15, 1987)
- K872542: Schneider-Shiley Softrac-Pta (TM) Angio. Catheter (Sep 14, 1987)
- K872472: Schneider-Shiley Biflator Balloon Inflation Device (Sep 14, 1987)
- K863342: Softip Coronary Sinus Cardioplegia Catheter (Mar 3, 1987)
- K861238: Angiomedics Cath Sheath Introduc W/Hemostasis Valv (Jul 16, 1986)
- K852872: Angiomedics Softip Catheter (Oct 11, 1985)
- K850271: Angiomedic's Catheter-Diagnostic Intravascular (Apr 3, 1985)
- K834275: Softip Catheter (Feb 4, 1984)

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