510(k) K973104 ยท KGI Densitometer, Bone
NORLAND MODEL PDEXA BONE DENSITOMETER
| Applicant | Norland Corp., Fort Atkinson WI, US |
| Decision | Substantially Equivalent, Jan 29, 1998 |
| Received | Aug 19, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973104
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.