Clearance Summary
RelieforMe TENS/EMS Device Model UPK-GE01 received FDA 510(k) clearance under submission number K192733, sponsored by Umeheal , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2019-12-23.
- Submission: K192733
- Applicant / Sponsor: Umeheal , Ltd.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5850
- Decision date: 2019-12-23
Classification & Regulation
This clearance is catalogued under FDA product code IPF and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.