Medical Device Manufacturer · US , St. Paul , MN

Bio-Vascular, Inc. - FDA 510(k) Cleared Devices

26 submissions · 25 cleared · Since 1986

26

Total

25

Cleared

0

Denied

FDA 510(k) Regulatory Record - Bio-Vascular, Inc. General & Plastic Surgery ✕

8 devices

1-8 of 8

Cleared Feb 22, 2000

PERI-STRIPS-SLEEVE, PERI-STRIPS-STRIP AND PERI-STRIPS DRY (NON-NAOH-TREATED...

General & Plastic Surgery · 208d

Cleared Oct 09, 1998

PERI-GUARD, CV PERI-GUARD, OCU-GUARD, SUPPLE PERI-GUARD, PERI-STRIPS -...

General & Plastic Surgery · 29d

Cleared May 09, 1997

PERI-STRIPS DRY - STAPLE LINE REINFORCEMENT

General & Plastic Surgery · 49d

Cleared Jun 13, 1996

SUPPLE PERI-GUARD PERICARDIUM

General & Plastic Surgery · 34d

Cleared Jun 13, 1996

PERI-GUARD PERICARDIUM

General & Plastic Surgery · 34d

Cleared Jul 08, 1994

PERI-STRIPS PLANAR CONFIGURATION STAPLE LINE REINFORCEMENT

General & Plastic Surgery · 37d

Cleared May 02, 1994

General & Plastic Surgery · 108d

Cleared Dec 21, 1992

SUPPLE PERI-GUARD

General & Plastic Surgery · 208d