510(k) K030734 ยท DYB Introducer, Catheter
PATHWAY ACCESS SHEATH CATHETER
| Applicant | Vertelink Corporation, Mission Viejo CA, US |
| Decision | Substantially Equivalent, Sep 10, 2003 |
| Received | Mar 10, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030734
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.