510(k) K933033 ยท DQY Catheter, Percutaneous
GUIDING CATHETER HEMOSTASIS VALVE CAP
| Applicant | Arrow Intl., Inc., Reading PA, US |
| Decision | Substantially Equivalent, Sep 10, 1993 |
| Received | Jun 22, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933033
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.