510(k) K990538 ยท HCC Device, Biofeedback
BRAINMASTER 2E MODULE AND SOFTWARE BIOFEEDBACK DEVICE
| Applicant | Brainmaster, Great Neck NY, US |
| Decision | Substantially Equivalent, May 19, 1999 |
| Received | Feb 19, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990538
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.