# Aries Medical, Inc.

- Location (FDA's records): Woburn, MA
- FDA decisions: 19 (1984–1991): 19 510(k) clearances
- Product codes: DSP (8), DYB (4), KFM (2), MJL (1), BSO (1), BSP (1), DSY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (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
- I-Flow Corp.: 2 (https://510kreport.com/company/i-flow)
- Rusch Intl.: 1 (https://510kreport.com/company/rusch-intl)
- Spinal Integration, LLC: 1 (https://510kreport.com/company/spinal-integration)
- Abbott Vascular: 1 (https://510kreport.com/company/abbott-vascular)

## Its most-cited devices
- K840202: Epidural Catheter (1984), cited by 3
- K840201: Epidural Catheter Tray (1984), cited by 1
- K840641: Vessel Dilator (1984), cited by 1

## Recent decisions
- K912604: SJM/Cad Isoflow (TM) Centrifugal Pump 2100CP, Modif (Oct 28, 1991)
- K903925: Aries Meldical Model 2100HC Hank Crank (Dec 21, 1990)
- K903442: Aries Taperseal (TM) Sheath (Aug 23, 1990)
- K895433: Aries 30CC & 50CC Intra-Aortic Balloon & Cont. Sys (Apr 10, 1990)
- K882289: Aries 40CC Percu. (D/L) Intra-Aortic Balloon Cath. (Dec 12, 1988)
- K864537: 40CC Percutaneous Pre-Furl (D/L) Balloon Catheter (Jun 19, 1987)
- K864994: 40CC Per. Pre-Furl (S/L) Intra-Aortic Catheter (Jun 19, 1987)
- K864567: 40CC Percutaneous Furl Dou. Lumen Balloon Catheter (May 12, 1987)

Source page: https://510kreport.com/company/aries-medical