510(k) K141809 ยท DRM Compressor, Cardiac, External
RMU-1000 AUTOMATED CHEST COMPRESSION SYSTEM
| Applicant | Defibtech, LLC, Guilford CT, US |
| Decision | Substantially Equivalent, Oct 27, 2014 |
| Received | Jul 7, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141809
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.