Summit Doppler Systems, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K103693 | VANTAGE ABI | DXN | 2011-02-15 | View |
| 510(k) | K101816 | STN PROBE | ITX | 2010-08-19 | View |
| 510(k) | K093393 | LIFEDOP MODEL 300ABI | JAF | 2009-12-24 | View |
| 510(k) | K090499 | LIFEDOP MODEL, L350R | MAA | 2009-03-31 | View |
| 510(k) | K063600 | VISTA AVS | JAF | 2006-12-19 | View |
| 510(k) | K060410 | ECHOHEART TRANSVAGINAL DOPPLER PROBE | HEK | 2006-04-10 | View |
| 510(k) | K024197 | LIFEDOP DOPPLER | KNG | 2003-01-03 | View |
No matching devices.
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