510(k) K001347 ยท GZO Device, Galvanic Skin Response Measurement
MERIDIAN-II AND MERDIAN-PLUS
| Applicant | Meridian Co., Ltd., Songpa-Gu, Seoul, KR |
| Decision | Substantially Equivalent, Nov 3, 2000 |
| Received | Apr 28, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001347
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.