510(k) K102166 ยท GZO Device, Galvanic Skin Response Measurement
ELECTRO INTERSTITIAL SCAN
| Applicant | Ld Technology, LLC, Miami FL, US |
| Decision | Substantially Equivalent, Dec 10, 2010 |
| Received | Aug 2, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102166
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.