510(k) K862121 ยท KZM Device, Muscle Monitoring
E.W.L. P-TENS/H-WAVE
| Applicant | Electronic Waveform Laboratory, Inc., Huntington Beach CA, US |
| Decision | Substantially Equivalent, Jun 17, 1987 |
| Received | Jun 3, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862121
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.