510(k) K030504 ยท MCW Catheter, Peripheral, Atherectomy
AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL 10060060
| Applicant | Idev Technologies, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Sep 16, 2003 |
| Received | Feb 19, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030504
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.