510(k) K150804 ยท GZO Device, Galvanic Skin Response Measurement
QBioScan
| Applicant | Medeia, Inc., Miami FL, US |
| Decision | Substantially Equivalent, Oct 19, 2015 |
| Received | Mar 26, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150804
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.