510(k) K200657 ยท LRK Device, Anti-Snoring
SmartGuard Anti-Snoring Device
| Applicant | Smartguard Rx, Inc., Layton UT, US |
| Decision | Substantially Equivalent, Aug 23, 2021 |
| Received | Mar 12, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200657
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.