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 R4 Vascular with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jun 6, 2013: VECTOR PTA BALLOON DILATATION CATHETER.
| Jun 6, 2013 | VECTOR PTA BALLOON DILATATION CATHETERK131329 · LIT | 510(k) clearances |
| Jun 14, 2012 | VECTORK121385 · LIT | 510(k) clearances |
| Feb 18, 2010 | DURASPAN HEMODIALYSIS LONG-TERM CATHETERK100169 · MSD | 510(k) clearances |
| Jan 8, 2010 | DURASPAN HEMODIALYSIS LONG-TERM CATHETER, MODELS 62152420, 621512820, 62153220, 62153620, 62154020, 62155520K091506 · MSD | 510(k) clearances |
| Nov 18, 2009 | PHEROCIOUS 10.5 FR (24 CM, 28 CM AND 32 CM), MODELS 430102440, 430102840, 430103240K092040 · LJS | 510(k) clearances |
| Mar 16, 2009 | ZEUS CT PICC 4 FR AND 5 FR SINGLE AND DUAL LUMENK083763 · LJS | 510(k) clearances |
| Aug 20, 2007 | R4 VASCULAR INC. PEGASUS CT PICC, MODEL 500005-001,002, 004, 005, 500004-001, 002,004,005K071361 · LJS | 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
