510(k) K130130 ยท LQZ Device, Jaw Repositioning
ATG/SM-OSA APPLIANCES
| Applicant | Selane Products, Inc., Bradenton FL, US |
| Decision | Substantially Equivalent, Aug 26, 2013 |
| Received | Jan 17, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130130
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.