Clearance Summary
LEVO MOBIL LCM received FDA 510(k) clearance under submission number K963817, sponsored by Levo USA. 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 1997-12-23.
- Submission: K963817
- Applicant / Sponsor: Levo USA
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.3900
- Decision date: 1997-12-23
Classification & Regulation
This clearance is catalogued under FDA product code IPL and 21 CFR 890.3900, within the Physical Medicine review panel as a Class II device.