510(k) K992392 ยท MUH System, X-Ray, Extraoral Source, Digital
RTLX
| Applicant | Infimed, Inc., Liverpool NY, US |
| Decision | Substantially Equivalent, Mar 31, 2000 |
| Received | Jul 19, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992392
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.