510(k) K802637 ยท IKN Electromyograph, Diagnostic
TECA MODEL-10 ELECTROMYOGRAPH
| Applicant | Teca, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 26, 1980 |
| Received | Oct 22, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802637
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.