510(k) K833879 ยท DRM Compressor, Cardiac, External
CARDIOPULMONARY RESUSCITATOR
| Applicant | Michigan Instruments, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 27, 1983 |
| Received | Nov 8, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833879
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.