510(k) K891021 ยท DXE Catheter, Embolectomy
TRI-LUMEN INTRA VASCULAR BALLOON CATHETER
| Applicant | Ideal Medical, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Sep 18, 1989 |
| Received | Feb 28, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891021
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.