510(k) K173553 ยท DRM Compressor, Cardiac, External
LUCAS 3 Chest Compression System
| Applicant | Jolife AB, Lund, SE |
| Decision | Substantially Equivalent, Feb 8, 2018 |
| Received | Nov 16, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173553
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.