# Scimed Peripheral Interventions

- Location (FDA's records): Plymouth, MN
- FDA decisions: 8 (1993–1995): 8 510(k) clearances
- Product codes: DQX (4), LIT (2), KRA (1), DQY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Phenox Limited: 1 (https://510kreport.com/company/phenox)
- Cordis Neurovascular, Inc.: 1 (https://510kreport.com/company/cordis-neurovascular)

## Its most-cited devices
- K945904: Scimed (R) Venture (TM) II Infusion Catheter (1995), cited by 1
- K934359: Scimed Strike Steerable Guide Wire (1993), cited by 1
- K934122: Scimed Transend EX Steerable Guide Wire and Accessories (1993), cited by 1

## Recent decisions
- K945904: Scimed (R) Venture (TM) II Infusion Catheter (May 19, 1995)
- K946272: Scimed (R) Courier Guide Catheter (Apr 17, 1995)
- K944677: Scimed Transent EX Steerable Guide Wire and Accessories (Feb 8, 1995)
- K941710: Scimed Transend Steerable Guide Wire and Accessories (Sep 1, 1994)
- K935501: Scimed Viper Pta Catheter with Bioslide Hydrophilic Coating (Jan 27, 1994)
- K934793: Scimed Maverick (Jan 5, 1994)
- K934359: Scimed Strike Steerable Guide Wire (Oct 7, 1993)
- K934122: Scimed Transend EX Steerable Guide Wire and Accessories (Oct 7, 1993)

Source page: https://510kreport.com/company/scimed-peripheral-interventions