510(k) K893903 ยท KQX Goniometer, Ac-Powered
KRONAMAX KUBE
| Applicant | Physicians Digital Co., Richmond CA, US |
| Decision | Substantially Equivalent, Nov 29, 1989 |
| Received | May 30, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893903
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.