510(k) K850082 ยท KQW Goniometer, Nonpowered
HAND HELD GONIOMETER
| Applicant | Chattanooga Group, Inc., Red Bank TN, US |
| Decision | Substantially Equivalent, Apr 4, 1985 |
| Received | Jan 10, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850082
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.