510(k) K882274 ยท DSP System, Balloon, Intra-Aortic And Control
10.5 FRENCH PERCUTANEOUS DOUBLE LUMEN INTRA-AORTIC
| Applicant | Kontron Instruments, Inc., Everett MA, US |
| Decision | Substantially Equivalent, Mar 20, 1989 |
| Received | May 31, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882274
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.