510(k) K071866 ยท HCC Device, Biofeedback
NTRAINER SYSTEM
| Applicant | Kcbiomedix, Inc., Lees Summit MO, US |
| Decision | Substantially Equivalent, Feb 1, 2008 |
| Received | Jul 6, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071866
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.