510(k) K963778 ยท EIA Unit, Operative Dental
CDR-CAM
| Applicant | Schick Technologies, Inc., Long Island City NY, US |
| Decision | Substantially Equivalent, Nov 22, 1996 |
| Received | Sep 20, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963778
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.