510(k) K993824 ยท GZO Device, Galvanic Skin Response Measurement
MSAS PROFESSIONAL
| Applicant | Biomeridian, Int., Draper UT, US |
| Decision | Substantially Equivalent, Jan 20, 2000 |
| Received | Nov 12, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K993824
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.