Clearance Summary
HeatLux Pro I received FDA 510(k) clearance under submission number K150175, sponsored by Home Skinovations , Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2015-03-31.
- Submission: K150175
- Applicant / Sponsor: Home Skinovations , Ltd.
- Clearance pathway: Special
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5500
- Decision date: 2015-03-31
Classification & Regulation
This clearance is catalogued under FDA product code ILY and 21 CFR 890.5500, within the Physical Medicine review panel as a Class II device.