510(k) K981844 ยท HCC Device, Biofeedback
SLEEP MANAGEMENT SYSTEM
| Applicant | Rmp, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Aug 7, 1998 |
| Received | May 26, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981844
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.