510(k) K010897 ยท GZO Device, Galvanic Skin Response Measurement
MERIDIAN-PORTABLE
| Applicant | Meridian Co., Ltd., Songpa-Gu, Seoul, KR |
| Decision | Substantially Equivalent, Jun 19, 2001 |
| Received | Mar 26, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010897
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.