510(k) K962237 ยท DRM Compressor, Cardiac, External
THUMPER CARDIOPULMONARY RESUSCITATOR
| Applicant | Michigan Instruments, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Sep 5, 1996 |
| Received | Jun 11, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962237
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.