510(k) K020360 ยท GZO Device, Galvanic Skin Response Measurement
ABR-2000
| Applicant | Meridian Co., Ltd., Songpa-Gu, Seoul, KR |
| Decision | Substantially Equivalent, Aug 29, 2002 |
| Received | Feb 4, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020360
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.