Medevice, Inc. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Medevice, Inc. has 4 FDA 510(k) cleared medical devices. Based in Canada L4w 4m2, CA.
Historical record: 4 cleared submissions from 1989 to 2007. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Medevice, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Dec 07, 2007
SIGHTSURE OPERATIONAL INDICATOR, MODEL SS301
Gastroenterology & Urology
88d
Cleared
Mar 26, 1993
BIO-MATE PIC CATHETER
General Hospital
408d
Cleared
Dec 17, 1991
MEDE-FLO I.V. EXTENSION SET
General Hospital
172d
Cleared
Mar 30, 1990
BIO-MATE(TM) PEDIATRIC EPIDURAL CATHETER
Anesthesiology
18d
Cleared
Jun 23, 1989
BIO-MATE(TM) EPIDURAL CATHETER
Anesthesiology
205d