510(k) K883852 ยท DXE Catheter, Embolectomy
CATHETER, CARDIOVASCULAR, BALLOON TYPE
| Applicant | Wb Intl., Inc., Miami FL, US |
| Decision | Substantially Equivalent, Dec 7, 1989 |
| Received | Sep 13, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883852
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.