510(k) K131568 ยท GZO Device, Galvanic Skin Response Measurement
SUDO PATH
| Applicant | Ld Technology, LLC, Miami FL, US |
| Decision | Substantially Equivalent, Jun 28, 2013 |
| Received | May 30, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131568
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.