510(k) K000162 ยท KGI Densitometer, Bone
METRISCAN BONE DENSITY SYSTEM
| Applicant | Alara, Inc., Hayward CA, US |
| Decision | Substantially Equivalent, May 12, 2000 |
| Received | Jan 19, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000162
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.