510(k) K100840 ยท DXE Catheter, Embolectomy
EMBO PLUS EMBOLECTOMY CATHETER
| Applicant | Hotspur Technologies, Mountain View CA, US |
| Decision | Substantially Equivalent, Jul 12, 2010 |
| Received | Mar 24, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100840
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.