510(k) K032105 ยท DWX Stripper, Artery, Intraluminal
ENDOHELIX ENDARTERECTOMY DEVICE
| Applicant | Endarx, Inc., Portola Valley CA, US |
| Decision | Substantially Equivalent, Oct 30, 2003 |
| Received | Jul 8, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032105
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.