510(k) K971735 ยท KGI Densitometer, Bone
ACCUDEXA BONE DENSITOMETER
| Applicant | Schick Technologies, Inc., Rockville MD, US |
| Decision | Substantially Equivalent, Dec 2, 1997 |
| Received | May 12, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971735
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.