510(k) K962577 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
ARROWGARD BLUE QUAD-LUMEN CENTRAL VENOUS CATHETER
| Applicant | Arrow Intl., Inc., Reading PA, US |
| Decision | Substantially Equivalent, Aug 21, 1997 |
| Received | Jul 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962577
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 24, 2009 | Arrow International Inc Arrow ARROWg+ard Quad-Lumen CVCs (Central Venous Catheters) Terminated |
FOZ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.