Bio-Vascular, Inc. - FDA 510(k) Cleared Devices
26
Total
25
Cleared
0
Denied
Bio-Vascular, Inc. has 25 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Historical record: 25 cleared submissions from 1986 to 2000. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Bio-Vascular, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Bio-Vascular, Inc.
26 devices
Cleared
Oct 13, 2000
BVI SLING
Obstetrics & Gynecology
81d
Cleared
Feb 22, 2000
PERI-STRIPS-SLEEVE, PERI-STRIPS-STRIP AND PERI-STRIPS DRY (NON-NAOH-TREATED...
General & Plastic Surgery
208d
Cleared
Nov 12, 1998
CV PERI-GUARD AND VASCU-GUARD
Cardiovascular
30d
Cleared
Nov 06, 1998
OCU-GUARD AND OCU-GUARD SUPPLE
Ophthalmic
24d
Cleared
Oct 09, 1998
PERI-GUARD, CV PERI-GUARD, OCU-GUARD, SUPPLE PERI-GUARD, PERI-STRIPS -...
General & Plastic Surgery
29d
Cleared
Aug 04, 1998
FLO-THRU
Cardiovascular
89d
Cleared
Jul 30, 1998
DURA-GUARD - DURAL REPAIR PATCH
Neurology
30d
Cleared
Apr 10, 1998
CV PERI-GUARD - CARDIOVASCULAR PATCH
Cardiovascular
336d
Cleared
Dec 24, 1997
DURA-GUARD-DURAL REPAIR PATCH
Neurology
86d
Cleared
Dec 16, 1997
OCU-GUARD ORBITAL IMPLANT WRAP, SUPPLE OCU-GUARD ORBITAL IMPLANT WRAP
Ophthalmic
88d
Cleared
May 09, 1997
PERI-STRIPS DRY - STAPLE LINE REINFORCEMENT
General & Plastic Surgery
49d
Cleared
Nov 27, 1996
ADVANCED DIAGNOSTIC VIEWER (ADV)
Radiology
72d