510(k) K993202 ยท GZO Device, Galvanic Skin Response Measurement
EIM-107 PREP-CHECK
| Applicant | General Devices, Ridgefield NJ, US |
| Decision | Substantially Equivalent, Dec 17, 1999 |
| Received | Sep 24, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993202
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.