Zyppah Anti-Snoring Device— 510(k) K182312
Substantially EquivalentAlways More Marketing
FDA 510(k) clearance K182312 for Zyppah Anti-Snoring Device, Substantially Equivalent on 2019-01-24. Applicant: Always More Marketing.
Clearance details
- Applicant
- Always More Marketing
- Product code
- Code LRK
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Calabasas, CA, US
Adverse events under product code LRK
product code LRK- Injury
- 246
- Malfunction
- 1,044
- Total
- 1,290
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.