Microvena Corp.
FDA 510(k) & PMA Approved Devices — 18 products
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Total Devices18
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K991898 | ULTRA-SELECT GUIDEWIRE, HYTEK GUIDEWIRE | DQX | 1999-06-16 | View |
| 510(k) | K991194 | MODIFICATION TO ULTRA-SELECT GUIDEWIRE | DQX | 1999-05-05 | View |
| 510(k) | K982657 | AMPLATZ THROMBECTOMY DEVICE MODELS ATD 601, ATD 602, ATD 801, ATD 802, FOOT PEDAL ASSEMBLY MODEL AK 100 | MCW | 1998-11-18 | View |
| 510(k) | K970668 | THE AMPLANTZ GOOSE NECK MICROSNARE | DQY | 1998-06-10 | View |
| 510(k) | K972511 | AMPLATZ GOOSE NECK SNARE KIT/ CATHETER | DXE | 1998-03-06 | View |
| 510(k) | K971984 | AMPLATZ THROMBECTOMY DEVICE(ATD 603,602,801,802)/FOOT PEDAL ASSEMBLY(AK 200) | MCW | 1997-09-19 | View |
| 510(k) | K954642 | HYDRO-SELECT GUIDEWIRE | DQX | 1996-12-17 | View |
| 510(k) | K954205 | THE AMPLATZ THROMBECTOMY DEVICE | MCW | 1996-08-13 | View |
| 510(k) | K955304 | CRICKET | DQX | 1996-05-16 | View |
| 510(k) | K952860 | THE NINER NITINOL GUIDEWIRE | DQX | 1995-12-13 | View |
| 510(k) | K946356 | M-PATH NITINOL GUIDEWIRE | DQX | 1995-03-31 | View |
| 510(k) | K925439 | MICROSNARE | DQY | 1993-09-24 | View |
| 510(k) | K922060 | .25' ULTRA-SELECT GUIDEWIRE | DQX | 1993-02-23 | View |
| 510(k) | K914046 | THE BIG EASY Y-ADAPTER | DYB | 1991-11-08 | View |
| 510(k) | K910280 | ULTRA-SELECT PTCA GUIDEWIRE | DQX | 1991-04-19 | View |
| 510(k) | K901502 | AMPLATZ GOOSE-NECK SNARE | DXE | 1990-12-03 | View |
| 510(k) | K900657 | UNIVERSAL DELIVERY SYSTEM CATHETER | DQY | 1990-05-09 | View |
| 510(k) | K896096 | SOLOSTICK (AMPLATZ DILATOR NEEDLE) | DRE | 1990-04-10 | View |
No matching devices.
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