510(k) K880310 ยท DXT Injector And Syringe, Angiographic
ANGIO DRAPE PACK ACP-010FM
| Applicant | Arrow Intl., Inc., Reading PA, US |
| Decision | Substantially Equivalent, Apr 22, 1988 |
| Received | Jan 25, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880310
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.