Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in CanadaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Becton DickinsonLabelled 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 Vas-Cath with 27 510(k) clearances. The most recent is a 510(k) clearance dated Jun 19, 1998: OPTI-PLAST (CENTURION) 5.5F ANGIOPLASTY CATHETER.
| Jun 19, 1998 | OPTI-PLAST (CENTURION) 5.5F ANGIOPLASTY CATHETERK973013 · LIT | 510(k) clearances |
| Aug 19, 1997 | NIAGARA DUAL LUMEN CATHETERK965178 · MPB | 510(k) clearances |
| May 28, 1997 | ULTRAVERSE PTA CATHETERK964881 · LIT | 510(k) clearances |
| May 9, 1997 | OPTI-PLAST XL 5.5 F PTA CATHETERK970725 · LIT | 510(k) clearances |
| Oct 18, 1994 | OPTI-PLAST ANGIOPLASTY CATHETERK941706 · LIT | 510(k) clearances |
| Mar 10, 1994 | VAS-CATH INC. OPTI-PLAST ANGIOPLASTY CATHETERK925485 · LIT | 510(k) clearances |
| Sep 24, 1993 | OPTI-PLAST 5F PTA CATHETERSK933483 · LIT | 510(k) clearances |
| Jul 1, 1993 | VAS-CATH DUALATOR(TM) VESSEL DILATORK914210 · FKA | 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
