510(k) K072439 ยท KGI Densitometer, Bone
GE LUNAR DPX & PRODIGY SERIES DEXA BONE DENSITOMETERS WITH MOBILE KIT
| Applicant | Ge Medical Systems Ultrasound and Primary Care Dia, Madison WI, US |
| Decision | Substantially Equivalent, Sep 14, 2007 |
| Received | Aug 30, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072439
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.