510(k) K823342 ยท DSP System, Balloon, Intra-Aortic And Control
PERCOR INTRA-AORTIC BALLOON INSERTION
| Applicant | Datascope Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 24, 1983 |
| Received | Nov 8, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823342
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.