510(k) K862128 ยท KQX Goniometer, Ac-Powered
DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER)
| Applicant | Health Products, Inc., Hauppauge NY, US |
| Decision | Substantially Equivalent, Jul 11, 1986 |
| Received | Jun 4, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862128
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.