Clearance Summary
Lite received FDA 510(k) clearance under submission number K172409, sponsored by Tzora Active Systems , 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 2018-05-02.
- Submission: K172409
- Applicant / Sponsor: Tzora Active Systems , Ltd.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.3800
- Decision date: 2018-05-02
Classification & Regulation
This clearance is catalogued under FDA product code INI and 21 CFR 890.3800, within the Physical Medicine review panel as a Class II device.