510(k) K031291 ยท MUH System, X-Ray, Extraoral Source, Digital
CDR PANX, MODEL 4792
| Applicant | Schick Technologies, Inc., Long Island City NY, US |
| Decision | Substantially Equivalent, May 5, 2003 |
| Received | Apr 23, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031291
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.