510(k) K982950 ยท IKT Electrode, Needle, Diagnostic Electromyograph
FINE WIRE ELECTRODE MMODEL NUMBERS 221-14-730, 221-24-730, 221-14-550, 221-24-550
| Applicant | Chalgren Enterprises, Inc., Gilroy CA, US |
| Decision | Substantially Equivalent, Jun 22, 1999 |
| Received | Aug 21, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982950
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.