510(k) K840037 ยท DSP System, Balloon, Intra-Aortic And Control
MODIFIED SMEC PERCUTANEOUS INTRA-AORTIC
| Applicant | Smec, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 1, 1985 |
| Received | Jan 5, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840037
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.