Peripheral Systems Group

17 FDA 510(k) medical device clearances.

Top product codes for Peripheral Systems Group

LIT — Cardiovascular 5 devices
ITX — Radiology 4 devices
DQO — Cardiovascular 2 devices
DQX — Cardiovascular 2 devices
DPW — Cardiovascular 1 device
DQY — Cardiovascular 1 device
KOE — Gastroenterology, Urology 1 device
KRA — Cardiovascular 1 device

Recent clearances by Peripheral Systems Group

K940804 — SMARTNEEDLE VASCULAR ACCESS SYSTEM, MODIFICATION ITX · 1994-06-10
K934433 — VANTAGE DIALTAION CATHETER LIT · 1993-12-09
K932777 — SMARTNEEDLE(R) OVER-THE-NEEDLE CATHETER ITX · 1993-10-07
K931327 — PSG DIRECTIONAL HYDROPHILIC GUIDE WIRE DQX · 1993-07-14
K915554 — HI-TORQUE SPORT-T(TM) GUIDE WIRE DQX · 1993-02-09
K914979 — EDM(R) INFUSION CATHETER KRA · 1992-09-16
K913941 — PSG(TM) 20 GUAGE DOPPLER NEEDLE ITX · 1992-02-27
K915168 — PROFLEX 5 LIT · 1992-02-19
K913477 — APEX(TM) PROSTATIC BALLOON DILATION CATHETER KOE · 1991-12-27
K913746 — SMARTNEEDLE(TM) VASCULAR ACCESS SYSTEM ITX · 1991-12-17
K904984 — ADVANCE 418(TM) LIT · 1991-04-12
K904959 — PSG HEMOSTATIC CONTROL VALVE DQO · 1990-12-17
K903625 — DOPPLER NEEDLE AND FLOW MONITOR DPW · 1990-11-07
K895179 — ACCESSOR PERIPHERAL DILATING GUIDE WIRE LIT · 1990-02-28
K894944 — BALLOON DILATATION CATHETER LIT · 1990-01-19
K895146 — GUIDING CATHETER DQO · 1990-01-19
K895932 — PSG(TM) EDM(TM) INFUSION CATHETER DQY · 1990-01-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.