510(k) K952221 ยท DSP System, Balloon, Intra-Aortic And Control
BSC/CA 30 & 40 SENSATION, MODELS 930 & 940
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Aug 11, 1995 |
| Received | May 12, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952221
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.