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 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Velocimed with 6 510(k) clearances. The most recent is a 510(k) clearance dated Sep 7, 2006: PROXIS SYSTEM.
| Date | Record | Source |
|---|---|---|
| Sep 7, 2006 | PROXIS SYSTEMK052523 · NFA | 510(k) clearances |
| May 2, 2005 | PREMERE DELIVERY SHEATH, MODEL PDSK043084 · DYB | 510(k) clearances |
| Jan 7, 2005 | PROXIS SYSTEM, MODEL EPS 101K042117 · DQY | 510(k) clearances |
| Nov 22, 2004 | VENTURE WIRE CONTROL CATHETER, MODEL WCCK042910 · DQY | 510(k) clearances |
| Aug 18, 2004 | VENTURE WIRE CONTROL CATHETERK040922 · DQY | 510(k) clearances |
| Aug 4, 2003 | PROXIS FLOW-CONTROL DEVICE, MODELS EPS 101, IC 101K023548 · DQY | 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
