510(k) K143310 ยท OBH Monitor, Extracellular Fluid, Lymphedema, Extremity
MoisturemeterD
| Applicant | Delfin Technologies, Ltd., Kuopio, FI |
| Decision | Substantially Equivalent, Nov 19, 2015 |
| Received | Nov 18, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143310
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.