510(k) K182312 ยท LRK Device, Anti-Snoring
Zyppah Anti-Snoring Device
| Applicant | Always More Marketing, Calabasas CA, US |
| Decision | Substantially Equivalent, Jan 24, 2019 |
| Received | Aug 27, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182312
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.