510(k) K220330 ยท LRK Device, Anti-Snoring
Soundly Anti Snoring Device
| Applicant | Greystone Ip, Ltd., Belfast, IE |
| Decision | Substantially Equivalent, Sep 8, 2022 |
| Received | Feb 4, 2022 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K220330
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.