510(k) K961645 ยท HCC Device, Biofeedback
MRS-2D
| Applicant | Lexicor Medical Technology, Inc., Boulder CO, US |
| Decision | Substantially Equivalent, Oct 31, 1996 |
| Received | Apr 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961645
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.