510(k) K891582 ยท KGI Densitometer, Bone
MODIFIED OSTEOANALYZER (# SPSHA110/220)
| Applicant | Osteon, Inc., Wahiawa HI, US |
| Decision | Substantially Equivalent, Sep 12, 1989 |
| Received | Mar 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891582
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.