510(k) K973477 ยท DXE Catheter, Embolectomy
BIOSENSORS EMBOLECTOMY CATHETER
| Applicant | Sunscope Intl., Inc., Newport Beach CA, US |
| Decision | Substantially Equivalent, Sep 4, 1998 |
| Received | Sep 15, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973477
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.