Peripheral Systems Group - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Peripheral Systems Group has 17 FDA 510(k) cleared cardiovascular devices. Based in Mountain View, US.
Historical record: 17 cleared submissions from 1990 to 1994.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
17 devices
Cleared
Jun 10, 1994
SMARTNEEDLE VASCULAR ACCESS SYSTEM, MODIFICATION
Radiology
123d
Cleared
Dec 09, 1993
VANTAGE DIALTAION CATHETER
Cardiovascular
87d
Cleared
Oct 07, 1993
SMARTNEEDLE(R) OVER-THE-NEEDLE CATHETER
Radiology
121d
Cleared
Jul 14, 1993
PSG DIRECTIONAL HYDROPHILIC GUIDE WIRE
Cardiovascular
120d
Cleared
Feb 09, 1993
HI-TORQUE SPORT-T(TM) GUIDE WIRE
Cardiovascular
426d
Cleared
Sep 16, 1992
EDM(R) INFUSION CATHETER
Cardiovascular
315d
Cleared
Feb 27, 1992
PSG(TM) 20 GUAGE DOPPLER NEEDLE
Radiology
176d
Cleared
Feb 19, 1992
PROFLEX 5
Cardiovascular
96d
Cleared
Dec 27, 1991
APEX(TM) PROSTATIC BALLOON DILATION CATHETER
Gastroenterology & Urology
144d
Cleared
Dec 17, 1991
SMARTNEEDLE(TM) VASCULAR ACCESS SYSTEM
Radiology
118d
Cleared
Apr 12, 1991
ADVANCE 418(TM)
Cardiovascular
161d
Cleared
Dec 17, 1990
PSG HEMOSTATIC CONTROL VALVE
Cardiovascular
42d