510(k) K033452 ยท IKN Electromyograph, Diagnostic
CWAS 1000
| Applicant | Fasstech, North Billerica MA, US |
| Decision | Substantially Equivalent, Nov 28, 2003 |
| Received | Oct 30, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033452
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.