510(k) K850482 ยท DSP System, Balloon, Intra-Aortic And Control
DATASCOPE 8.5 FRENCH ELECTRODE INTRA-AORTIC BALLOO
| Applicant | Datascope Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, Aug 22, 1985 |
| Received | Feb 7, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850482
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.