510(k) K932268 ยท DSP System, Balloon, Intra-Aortic And Control
MODIFICATIONS TO INTRA-AORTIC BALLOONS
| Applicant | Kontron Instruments, Inc., Everett MA, US |
| Decision | Substantially Equivalent, Dec 15, 1993 |
| Received | Mar 31, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932268
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.