510(k) K926000 ยท DSP System, Balloon, Intra-Aortic And Control
9.5 FR SIDEWINDER DL INTRA-AORTIC BALLON CATHETER
| Applicant | Boston Scientific Corp, San Jose CA, US |
| Decision | Substantially Equivalent, Aug 30, 1993 |
| Received | Nov 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926000
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.