510(k) K894942 ยท DSP System, Balloon, Intra-Aortic And Control
SIDEWINDER 40CC DL INTRA-AORTIC BALLOON CATHETER
| Applicant | Boston Scientific Corp, Watertown MA, US |
| Decision | Substantially Equivalent, Sep 26, 1989 |
| Received | Aug 3, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894942
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.