510(k) K161919 ยท MUA Bone Sonometer
UltraScan 650
| Applicant | Cyberlogic, Inc., New York NY, US |
| Decision | Substantially Equivalent, Apr 5, 2017 |
| Received | Jul 13, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161919
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.