510(k) K201719 ยท LRK Device, Anti-Snoring
Vital Sleep
| Applicant | The Snore Reliever Company, LLC, North Bergen NJ, US |
| Decision | Substantially Equivalent, Jan 14, 2021 |
| Received | Jun 23, 2020 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K201719
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.