510(k) K820166 ยท DSP System, Balloon, Intra-Aortic And Control
ADAPTATION OF KANTRON 40 CC. PDLIAB
| Applicant | Kontron Instruments, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Apr 29, 1982 |
| Received | Jan 21, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820166
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.