510(k) K951019 ยท EIA Unit, Operative Dental
INTRAORAL VIDEO SCOPE AND WINDOW TUBE
| Applicant | Cuda Products Co., Jacksonville FL, US |
| Decision | Substantially Equivalent, May 10, 1995 |
| Received | Mar 7, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951019
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.