Clearance Summary
MPowRx Snoring Solution (also known as Good Morning Snore Solution) received FDA 510(k) clearance under submission number K193239, sponsored by Mpowrx Health and Wellness Products 2012, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2020-01-03.
- Submission: K193239
- Applicant / Sponsor: Mpowrx Health and Wellness Products 2012, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.5570
- Decision date: 2020-01-03
Classification & Regulation
This clearance is catalogued under FDA product code LRK and 21 CFR 872.5570, within the Dental review panel as a Class II device.