510(k) K180782 ยท KGI Densitometer, Bone
Aria
| Applicant | GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC, Madison WI, US |
| Decision | Substantially Equivalent, Apr 20, 2018 |
| Received | Mar 26, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180782
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.