510(k) K140342 ยท KGI Densitometer, Bone
QCT PRO ASYNCHRONOUS CALIBRATION MODULE, CLINIQCT
| Applicant | Mindways Software, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Aug 29, 2014 |
| Received | Feb 11, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140342
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.