510(k) K973219 ยท KPR System, X-Ray, Stationary
AMBER DU
| Applicant | Oldelft Corp. of America, Columbia MD, US |
| Decision | Substantially Equivalent, Oct 8, 1997 |
| Received | Aug 27, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973219
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.