510(k) K780541 ยท IKN Electromyograph, Diagnostic
PRESSURE MODULES MODELS 1855 & 1856
| Applicant | Life-Tech Instruments, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 19, 1978 |
| Received | Apr 3, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780541
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.