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., 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 15, 2026, FDA's public records list Becton Dickinson Vascular Access with 25 510(k) clearances. The most recent is a 510(k) clearance dated Dec 24, 1997: INSYTE, INSYTE-W, INSYTE AUTOGUARD CATHETERS.
| Dec 24, 1997 | INSYTE, INSYTE-W, INSYTE AUTOGUARD CATHETERSK971339 · FOZ | 510(k) clearances |
| Apr 8, 1997 | E-Z SET INFUSION SET/SAF-T E-Z SET INFUSION SETK970259 · FPA | 510(k) clearances |
| Jan 6, 1997 | FIRST MIDCATH CATHETER KITK964048 · FOZ | 510(k) clearances |
| Jan 6, 1997 | FIRST MIDCATH CATHETER WITH DUAL LUMENSK964049 · FOZ | 510(k) clearances |
| Jan 6, 1997 | FIRST MIDCATH CATHETERK964050 · FOZ | 510(k) clearances |
| Apr 8, 1996 | FIRST PICC INTRODUCER CATHETERK954906 · DYB | 510(k) clearances |
| Jul 31, 1995 | ANGIOCATH & INSYTE AUTOGUARD CATHETERSK952861 · FOZ | 510(k) clearances |
| Jul 31, 1995 | ANGIOCATH, NOVBALON, ANGIO-SET INTRAVASCULAR & ANGIOCATH INTRODUCTION DRAINAGE CATHETERK952757 · FOZ | 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
