510(k) K073079 ยท DRM Compressor, Cardiac, External
THUMPER, MODEL: 1008
| Applicant | Michigan Instruments, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Feb 14, 2008 |
| Received | Oct 31, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073079
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.