510(k) K920038 ยท HCC Device, Biofeedback
NEUROSEARCH-4
| Applicant | Lexicor, Boulder CO, US |
| Decision | Substantially Equivalent, Feb 8, 1995 |
| Received | Jan 6, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920038
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.