510(k) K851139 ยท DRM Compressor, Cardiac, External
THUMPER CARDIOPULMONARY RESUSCITATOR 1005
| Applicant | Michigan Instruments, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, May 15, 1985 |
| Received | Mar 21, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851139
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.