510(k) K033147 ยท MUH System, X-Ray, Extraoral Source, Digital
CLEARTOOTH DIGITAL X-RAY SYSTEM
| Applicant | Cleartooth Electronics, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Dec 30, 2003 |
| Received | Sep 30, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033147
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.