FDA 510(k) Applications Submitted by BIO-VASCULAR, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K971048 |
03/21/1997 |
PERI-STRIPS DRY - STAPLE LINE REINFORCEMENT |
BIO-VASCULAR, INC. |
K971726 |
05/09/1997 |
CV PERI-GUARD - CARDIOVASCULAR PATCH |
BIO-VASCULAR, INC. |
K973706 |
09/29/1997 |
DURA-GUARD-DURAL REPAIR PATCH |
BIO-VASCULAR, INC. |
K961810 |
05/10/1996 |
SUPPLE PERI-GUARD PERICARDIUM |
BIO-VASCULAR, INC. |
K961811 |
05/10/1996 |
PERI-GUARD PERICARDIUM |
BIO-VASCULAR, INC. |
K963697 |
09/16/1996 |
ADVANCED DIAGNOSTIC VIEWER (ADV) |
BIO-VASCULAR, INC. |
K981624 |
05/07/1998 |
FLO-THRU |
BIO-VASCULAR, INC. |
K002233 |
07/24/2000 |
BVI SLING |
BIO-VASCULAR, INC. |
K983162 |
09/10/1998 |
PERI-GUARD, CV PERI-GUARD, OCU-GUARD, SUPPLE PERI-GUARD, PERI-STRIPS - SLEEVE, PERI-STRIPS-STRIPS, PERI-STRIPS DRY, VASC |
BIO-VASCULAR, INC. |
K983581 |
10/13/1998 |
OCU-GUARD AND OCU-GUARD SUPPLE |
BIO-VASCULAR, INC. |
K983602 |
10/13/1998 |
CV PERI-GUARD AND VASCU-GUARD |
BIO-VASCULAR, INC. |
K973552 |
09/19/1997 |
OCU-GUARD ORBITAL IMPLANT WRAP, SUPPLE OCU-GUARD ORBITAL IMPLANT WRAP |
BIO-VASCULAR, INC. |
K982282 |
06/30/1998 |
DURA-GUARD - DURAL REPAIR PATCH |
BIO-VASCULAR, INC. |
K992537 |
07/29/1999 |
PERI-STRIPS-SLEEVE, PERI-STRIPS-STRIP AND PERI-STRIPS DRY (NON-NAOH-TREATED AND NAOH-TREATED |
BIO-VASCULAR, INC. |
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