Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Summit Doppler Systems with 7 510(k) clearances. The most recent is a 510(k) clearance dated Feb 15, 2011: VANTAGE ABI.
| Date | Record | Source |
|---|---|---|
| Feb 15, 2011 | VANTAGE ABIK103693 · DXN | 510(k) clearances |
| Aug 19, 2010 | STN PROBEK101816 · ITX | 510(k) clearances |
| Dec 24, 2009 | LIFEDOP MODEL 300ABIK093393 · JAF | 510(k) clearances |
| Mar 31, 2009 | LIFEDOP MODEL, L350RK090499 · MAA | 510(k) clearances |
| Dec 19, 2006 | VISTA AVSK063600 · JAF | 510(k) clearances |
| Apr 10, 2006 | ECHOHEART TRANSVAGINAL DOPPLER PROBEK060410 · HEK | 510(k) clearances |
| Jan 3, 2003 | LIFEDOP DOPPLERK024197 · KNG | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
