# Scimed

- Location (FDA's records): Maple Grove, MN
- FDA decisions: 8 (1990–1999): 8 510(k) clearances
- Product codes: DQO (2), DQX (2), LIT (1), MAV (1), DTR (1), DQY (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: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medtronic Cardiac Surgery, Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic-cardiac-surgery-medtronic)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Lifestream Int'L, Inc.: 1 (https://510kreport.com/company/lifestream-int-l)
- Minntech Corp.: 1 (https://510kreport.com/company/minntech)
- Quest Medical, Inc.: 1 (https://510kreport.com/company/quest-medical)

## Its most-cited devices
- K904171: Scimed Cardiotherm Cardioplegia Delivery System (1990), cited by 4
- K922706: Scimed Sideliner (1992), cited by 1

## Recent decisions
- K992142: Scimed Angiographic Catheters (Jul 21, 1999)
- K953909: Scimed 6 French Micro-Max Guide Catheter (Nov 13, 1995)
- K931584: Scimed Transport Steerable Guide Wire and Access. (Jul 1, 1993)
- K922706: Scimed Sideliner (Dec 10, 1992)
- K915347: Scimed Viper Catheter (Aug 17, 1992)
- K910987: 7FR. and 8FR. Triguide Guiding Catheter Add. Curve (May 29, 1991)
- K904171: Scimed Cardiotherm Cardioplegia Delivery System (Dec 6, 1990)
- K903503: Scimed Encore Inflation Device, Model SM2500 (Oct 9, 1990)

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