Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 14, 2026, FDA's public records list Vascular Control Systems with 9 510(k) clearances. The most recent is a 510(k) clearance dated Apr 21, 2006: BURBANK TENACULUM.
| Apr 21, 2006 | BURBANK TENACULUMK060573 · HDC | 510(k) clearances |
| Sep 6, 2005 | VCS DOPPLER TRANSCEIVER, MODEL 09-0023-01K052209 · DPW | 510(k) clearances |
| Feb 9, 2004 | CSTAT, MODELS 09-0014-01 AND 09-0014-02K032125 · DXC | 510(k) clearances |
| Dec 12, 2003 | TRANSVAGINAL DOPPLER CLAMP, MODELS: 09-0016-01, 09-0016-02, 09-0016-03K031812 · DXC | 510(k) clearances |
| May 9, 2003 | TRANSVAGINAL DOPPLER PROBEK031358 · ITX | 510(k) clearances |
| Jan 24, 2003 | BURBANK TENACULUM, MODEL 09-0011-01K030078 · HDC | 510(k) clearances |
| Dec 20, 2002 | VCS-A SERIES CLAMP WITH DOPPLER ULTRASOUND, MODEL 09-0007-01 AND 09-0007-02K023154 · DXC | 510(k) clearances |
| Sep 26, 2002 | TRANSVAGINAL DOPPLER PROBE, MODEL 09-0006-02K023024 · ITX | 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
