510(k) K922942 ยท EIA Unit, Operative Dental
PRO-SCOPE MODEL # PS-4000
| Applicant | Pro-Den Systems, Inc., Portland OR, US |
| Decision | Substantially Equivalent, Sep 10, 1993 |
| Received | Jun 18, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922942
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.