# Peripheral Systems Group

- Location (FDA's records): Mountain View, CA
- FDA decisions: 17 (1990–1994): 17 510(k) clearances
- Product codes: LIT (5), ITX (4), DQX (2), DQO (2), KOE (1), DPW (1), KRA (1), DQY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 12 (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
- Cardiovascular Dynamics, Inc.: 8 (https://510kreport.com/company/cardiovascular-dynamics)
- Guidant Corp.: 2 (https://510kreport.com/company/guidant)
- Mallinckroot, Inc.: 1 (https://510kreport.com/company/mallinckroot)
- Argomed, Inc.: 1 (https://510kreport.com/company/argomed)

## Its most-cited devices
- K940804: Smartneedle Vascular Access System, Modification (1994), cited by 2
- K913746: Smartneedle (TM) Vascular Access System (1991), cited by 2
- K913941: PSG (TM) 20 Guage Doppler Needle (1992), cited by 2
- K903625: Doppler Needle and Flow Monitor (1990), cited by 2
- K915554: HI-Torque Sport-T (TM) Guide Wire (1993), cited by 1
- K904984: Advance 418(TM) (1991), cited by 1

## Recent decisions
- K940804: Smartneedle Vascular Access System, Modification (Jun 10, 1994)
- K934433: Vantage Dialtaion Catheter (Dec 9, 1993)
- K932777: Smartneedle (R) Over-the-Needle Catheter (Oct 7, 1993)
- K931327: PSG Directional Hydrophilic Guide Wire (Jul 14, 1993)
- K915554: HI-Torque Sport-T (TM) Guide Wire (Feb 9, 1993)
- K914979: Edm (R) Infusion Catheter (Sep 16, 1992)
- K913941: PSG (TM) 20 Guage Doppler Needle (Feb 27, 1992)
- K915168: Proflex 5 (Feb 19, 1992)

Source page: https://510kreport.com/company/peripheral-systems-group