510(k) K032962 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
AC 3 LUMEN CENTRAL VENOUS ACCESS KIT WITH ARROWG+ARD ANTIMICROBIAL SURFACE
| Applicant | Arrow Intl., Inc., Reading PA, US |
| Decision | Substantially Equivalent, Oct 29, 2003 |
| Received | Sep 23, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K032962
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.