510(k) K901290 ยท LBB Dynamometer, Ac-Powered
ELECTRO-GONIOMETER DIAGNOSTIC DEVICE
| Applicant | Chattanooga Group, Inc., Hixson TN, US |
| Decision | Substantially Equivalent, Oct 1, 1990 |
| Received | Mar 20, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901290
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.