510(k) K011823 ยท HCC Device, Biofeedback
BIOREHAB SYSTEM
| Applicant | Nicolet Biomedical, Inc., Stoughton WI, US |
| Decision | Substantially Equivalent, Sep 6, 2001 |
| Received | Jun 11, 2001 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K011823
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.