510(k) K001429 ยท KGI Densitometer, Bone
MODIFICATION TO ACCUDEXA BONE DENSITOMETER
| Applicant | Schick Technologies, Inc., Long Island City NY, US |
| Decision | Substantially Equivalent, May 26, 2000 |
| Received | May 5, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001429
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.