510(k) K905313 ยท DSP System, Balloon, Intra-Aortic And Control
KONTRON INTRA-AORTIC BALLOON PUMP, MODEL KAAT II
| Applicant | Kontron Instruments, Inc., Everett MA, US |
| Decision | Substantially Equivalent, Jun 19, 1991 |
| Received | Nov 28, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905313
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.