510(k) K990049 ยท MUH System, X-Ray, Extraoral Source, Digital
CD-DENT DIGITAL IMAGING DEVICES FOR DENTAL X-RAY SYSTEMS, MODELS 600, 1000 AND 2000
| Applicant | Digident , Ltd., North Attleboro MA, US |
| Decision | Substantially Equivalent, Mar 12, 1999 |
| Received | Jan 7, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990049
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.