510(k) K931996 ยท KGI Densitometer, Bone
MODEL PDEXA BONE DENSITOMETER
| Applicant | Norland Corp., Fort Atkinson WI, US |
| Decision | Substantially Equivalent, Feb 1, 1995 |
| Received | Apr 23, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931996
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.