510(k) K091410 ยท IKT Electrode, Needle, Diagnostic Electromyograph
DISPOSABLE EMG NEEDLE ELECTRODES, MYOLINE, MYOLINE 2, MYOBOT,
| Applicant | Spes Medica Srl, Battipaglia, IT |
| Decision | Substantially Equivalent, Aug 11, 2009 |
| Received | May 13, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091410
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.