Scimed Peripheral Interventions is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Scimed Peripheral Interventions - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Scimed Peripheral Interventions has 8 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 8 cleared submissions from 1993 to 1995. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Scimed Peripheral Interventions Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Scimed Peripheral Interventions
8 devices
Cleared
May 19, 1995
SCIMED(R) VENTURE(TM) II INFUSION CATHETER
Cardiovascular
168d
Cleared
Apr 17, 1995
SCIMED(R) COURIER GUIDE CATHETER
Cardiovascular
115d
Cleared
Feb 08, 1995
SCIMED TRANSENT EX STEERABLE GUIDE WIRE AND ACCESSORIES
Cardiovascular
139d
Cleared
Sep 01, 1994
SCIMED TRANSEND STEERABLE GUIDE WIRE AND ACCESSORIES
Cardiovascular
148d
Cleared
Jan 27, 1994
SCIMED VIPER PTA CATHETER WITH BIOSLIDE HYDROPHILIC COATING
Cardiovascular
72d
Cleared
Jan 05, 1994
SCIMED MAVERICK
Cardiovascular
91d
Cleared
Oct 07, 1993
SCIMED TRANSEND EX STEERABLE GUIDE WIRE AND ACCESSORIES
Cardiovascular
43d
Cleared
Oct 07, 1993
SCIMED STRIKE STEERABLE GUIDE WIRE
Cardiovascular
29d