510(k) K012011 ยท HCC Device, Biofeedback
MODIFICATION TO A620 EEG
| Applicant | Stoelting Co., Wood Dale IL, US |
| Decision | Substantially Equivalent, Oct 10, 2001 |
| Received | Jun 28, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012011
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.