510(k) K974863 ยท KPR System, X-Ray, Stationary
IMIX DIGITAL THORAX SYSTEM
| Applicant | Advanced Instrument Development, Inc., Melrose Park IL, US |
| Decision | Substantially Equivalent, Mar 17, 1998 |
| Received | Dec 29, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974863
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.