510(k) K970436 ยท GZO Device, Galvanic Skin Response Measurement
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| Applicant | Natural Herbal Products, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Aug 15, 1997 |
| Received | Feb 5, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970436
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.