Maquet Cardiovascular, LLC
FDA 510(k) & PMA Approved Devices — 14 products
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Total Devices14
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K252445 | Fusion Bioline Vascular Graft | DSY | 2026-04-27 | View |
| 510(k) | K251238 | Vasoview Hemopro 3 Endoscopic Vessel Harvesting System (VH-6000); Vasoview Hemopro 3 Endoscopic Vessel Harvesting System with Vasoshield (VH-6001); Vasoview Hemopro 3 Power Supply (VH-6010) | GEI | 2025-05-30 | View |
| 510(k) | K243918 | Vasoview Hemopro 3 Power Supply | GEI | 2025-02-26 | View |
| 510(k) | K233879 | Vasoview Hemopro 3 Endoscopic Vessel Harvesting System (VH-6000), Vasoview Hemopro 3 Endoscopic Vessel Harvesting System with Vasoshield (VH-6001), Vasoview Hemopro 3 Power Adapter (VH-6020) | GEI | 2024-02-27 | View |
| 510(k) | K191930 | 7 mm Extended Length Endoscope | GCJ | 2020-04-15 | View |
| 510(k) | K191947 | VASOVIEW HEMOPRO Extension Cable, VASOVIEW HEMOPRO 2 Extension Cable, Bipolar Extension Cable, Fixed Distance, Active Return Cord | GEI | 2019-09-17 | View |
| 510(k) | K153194 | VASOVIEW HemoPro Endoscopic Vessel Harvesting System | GEI | 2016-04-19 | View |
| 510(k) | K153523 | FUSION Vascular Graft | DSY | 2016-02-16 | View |
| 510(k) | K132743 | HARVESTING CANNULA | GEI | 2013-12-03 | View |
| 510(k) | K131778 | FUSION VASCULAR GRAFT AND FUSION BIOLINE VASCULAR GRAFT | DSY | 2013-11-14 | View |
| 510(k) | K122612 | HEMASHIELD WOVEN DOUBLE VELOUR VASCULAR GRAFT MODEL M00202175XXXXX; M00202166XXXXX | MAL | 2012-09-10 | View |
| 510(k) | K101274 | VASOVIEW HEMOPRO 2 ENDOSCOPIC VESSEL HARVESTING SYSTEM | GEI | 2010-06-11 | View |
| 510(k) | K091733 | VASOVIEW 6 PRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-2500 | GEI | 2009-08-28 | View |
| 510(k) | K082725 | GRAFTGUARD PRESSURE CONTROLLING SYRINGE | GBX | 2008-12-17 | View |
No matching devices.
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