Bio-Vascular, Inc.
FDA 510(k) & PMA Approved Devices — 26 products
Advertisement
Total Devices26
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K002233 | BVI SLING | PAJ | 2000-10-13 | View |
| 510(k) | K992537 | PERI-STRIPS-SLEEVE, PERI-STRIPS-STRIP AND PERI-STRIPS DRY (NON-NAOH-TREATED AND NAOH-TREATED | FTM | 2000-02-22 | View |
| 510(k) | K983602 | CV PERI-GUARD AND VASCU-GUARD | DXZ | 1998-11-12 | View |
| 510(k) | K983581 | OCU-GUARD AND OCU-GUARD SUPPLE | HQX | 1998-11-06 | View |
| 510(k) | K983162 | PERI-GUARD, CV PERI-GUARD, OCU-GUARD, SUPPLE PERI-GUARD, PERI-STRIPS - SLEEVE, PERI-STRIPS-STRIPS, PERI-STRIPS DRY, VASC | FTM | 1998-10-09 | View |
| 510(k) | K981624 | FLO-THRU | DXC | 1998-08-04 | View |
| 510(k) | K982282 | DURA-GUARD - DURAL REPAIR PATCH | GXQ | 1998-07-30 | View |
| 510(k) | K971726 | CV PERI-GUARD - CARDIOVASCULAR PATCH | DXZ | 1998-04-10 | View |
| 510(k) | K973706 | DURA-GUARD-DURAL REPAIR PATCH | GXQ | 1997-12-24 | View |
| 510(k) | K973552 | OCU-GUARD ORBITAL IMPLANT WRAP, SUPPLE OCU-GUARD ORBITAL IMPLANT WRAP | MTZ | 1997-12-16 | View |
| 510(k) | K971048 | PERI-STRIPS DRY - STAPLE LINE REINFORCEMENT | FTM | 1997-05-09 | View |
| 510(k) | K963697 | ADVANCED DIAGNOSTIC VIEWER (ADV) | LLZ | 1996-11-27 | View |
| 510(k) | K961810 | SUPPLE PERI-GUARD PERICARDIUM | FTM | 1996-06-13 | View |
| 510(k) | K961811 | PERI-GUARD PERICARDIUM | FTM | 1996-06-13 | View |
| 510(k) | K950956 | DURA-GUARD DURAL REPAIR PATCH, DURA-GUARD DURA SUBSTITUTE | GXQ | 1995-06-02 | View |
| 510(k) | K942812 | FLO-RESTER DISPOSABLE VESSEL OCCLUDER | DXC | 1994-08-01 | View |
| 510(k) | K942583 | PERI-STRIPS PLANAR CONFIGURATION STAPLE LINE REINFORCEMENT | FTL | 1994-07-08 | View |
| 510(k) | K942010 | VASCU-GUARD | DXZ | 1994-07-07 | View |
| 510(k) | K940205 | PERI-STRIPS | FTM | 1994-05-02 | View |
| 510(k) | K923657 | SUPPLE PERI-GUARD | FTM | 1992-12-21 | View |
No matching devices.
Advertisement