510(k) K812908 ยท KQX Goniometer, Ac-Powered
ELECTRO-GONIOMETER
| Applicant | Chattanooga Group, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Nov 24, 1981 |
| Received | Oct 19, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812908
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.