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 15, 2026, FDA's public records list Catheter Innovations, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jun 6, 2002: VAXCEL PICC WITH PASV VALVE TECHNOLOGY.
| Jun 6, 2002 | VAXCEL PICC WITH PASV VALVE TECHNOLOGYK021704 · LJS | 510(k) clearances |
| Feb 28, 2001 | DUAL LUMEN MIDLINE CATHETERK010349 · LJS | 510(k) clearances |
| Dec 20, 2000 | PLACEMENT-PLUSK003642 · LJS | 510(k) clearances |
| Dec 3, 1999 | CATHETER INNOVATIONS IMPLANTABLE PORTK993860 · LJT | 510(k) clearances |
| Oct 21, 1999 | CATHETER INNOVATIONS IMPLANTABLE PORTK991897 · LJT | 510(k) clearances |
| May 1, 1998 | PASV DUAL LUMEN PERIPHERALLY INSERTED CENTRAL CATHETER (PICC) MODEL NUMBER PIC-NUMEROUSK981368 · FOZ | 510(k) clearances |
| May 1, 1998 | PASV DUAL LUMEN PERIPHERALLY INSERTED MIDLINE CATHETER MODEL NUMBER MIDLINE-NUMEROUSK981382 · FOZ | 510(k) clearances |
| Mar 11, 1998 | 6 INCH MINI-BONE EXTENSION SET WITH LUER LOCK, NES01S, 6 INCH MIN-BONE EXTENSION SET WITH LUER SLIP, NES02S, 6 INCH STATK980127 · FPA | 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
