510(k) K893243 ยท DSP System, Balloon, Intra-Aortic And Control
INTRA AORTIC BALLOON
| Applicant | Datascope Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, Jun 20, 1989 |
| Received | Jun 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893243
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.