510(k) K961212 ยท KQX Goniometer, Ac-Powered
SPINAL TOUCH
| Applicant | Fasstech, Burlington MA, US |
| Decision | Substantially Equivalent, Jun 12, 1996 |
| Received | Mar 28, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961212
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.