Clearance Summary
Rapid Hair Removal Pads received FDA 510(k) clearance under submission number K150349, sponsored by Full Power Aed. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2015-07-14.
- Submission: K150349
- Applicant / Sponsor: Full Power Aed
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5300
- Decision date: 2015-07-14
Classification & Regulation
This clearance is catalogued under FDA product code LDD and 21 CFR 870.5300, within the Cardiovascular review panel as a Class II device.