510(k) K972053 ยท KGI Densitometer, Bone
PIXI YOUNG ADULT REFERENC POPULATION FOR OS CALCIS AND FOREARM
| Applicant | Lunar Corp., Madison WI, US |
| Decision | Substantially Equivalent, Aug 8, 1997 |
| Received | Jun 2, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972053
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.