510(k) K161832 ยท LRK Device, Anti-Snoring
O2VENT T
| Applicant | Oventus Manufacturing Pty, Ltd., Indooroopilly, AU |
| Decision | Substantially Equivalent, Sep 23, 2016 |
| Received | Jul 5, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161832
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.