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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