510(k) K913078 ยท KGI Densitometer, Bone
LATERAL SPINE OPT. XR-SERIES X-RAY BONE DENSITOMET
| Applicant | Norland Corp., Fort Atkinson WI, US |
| Decision | Substantially Equivalent, Sep 24, 1991 |
| Received | Jul 11, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913078
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.