510(k) K112627 ยท LQZ Device, Jaw Repositioning
MILLENIUM ANTI-SNORING DEVICE
| Applicant | Millenium Dental Laboratory, Inc., Ramsey MN, US |
| Decision | Substantially Equivalent, Jun 6, 2012 |
| Received | Sep 9, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112627
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.