Peripheral Systems Group
Peripheral Systems Group holds FDA 510(k) medical device clearances, first cleared 1990, most recent 1994.
Top product codes for Peripheral Systems Group
Recent clearances by Peripheral Systems Group
- K940804 — SMARTNEEDLE VASCULAR ACCESS SYSTEM, MODIFICATION
- K934433 — VANTAGE DIALTAION CATHETER
- K932777 — SMARTNEEDLE(R) OVER-THE-NEEDLE CATHETER
- K931327 — PSG DIRECTIONAL HYDROPHILIC GUIDE WIRE
- K915554 — HI-TORQUE SPORT-T(TM) GUIDE WIRE
- K914979 — EDM(R) INFUSION CATHETER
- K913941 — PSG(TM) 20 GUAGE DOPPLER NEEDLE
- K915168 — PROFLEX 5
- K913477 — APEX(TM) PROSTATIC BALLOON DILATION CATHETER
- K913746 — SMARTNEEDLE(TM) VASCULAR ACCESS SYSTEM
- K904984 — ADVANCE 418(TM)
- K904959 — PSG HEMOSTATIC CONTROL VALVE
- K903625 — DOPPLER NEEDLE AND FLOW MONITOR
- K895179 — ACCESSOR PERIPHERAL DILATING GUIDE WIRE
- K894944 — BALLOON DILATATION CATHETER
- K895146 — GUIDING CATHETER
- K895932 — PSG(TM) EDM(TM) INFUSION CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.