Clearance Summary
3B Laser 500, 3B Laser 200, LA-X P 500, LA-X P 200 received FDA 510(k) clearance under submission number K142722, sponsored by Livetec GmbH. 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 2015-01-13.
- Submission: K142722
- Applicant / Sponsor: Livetec GmbH
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5500
- Decision date: 2015-01-13
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.