510(k) K062401 ยท DRM Compressor, Cardiac, External
MODIFICATION TO LUCAS
| Applicant | Jolife AB, Washington DC, US |
| Decision | Substantially Equivalent, Sep 28, 2006 |
| Received | Aug 16, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062401
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.