510(k) K970224 ยท KGI Densitometer, Bone
PIXI BONE DENSITOMETER
| Applicant | Lunar Corp., Madison WI, US |
| Decision | Substantially Equivalent, Apr 16, 1997 |
| Received | Jan 21, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970224
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.