510(k) K992129 ยท GZO Device, Galvanic Skin Response Measurement
PHAZX VLD-100
| Applicant | Phazx Systems, Inc., Boulder CO, US |
| Decision | Substantially Equivalent, Sep 17, 1999 |
| Received | Jun 23, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992129
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.