Clearance Summary
LIC-ORTHION MULTI-THERAPY TREATMENT TABLE received FDA 510(k) clearance under submission number K862022, sponsored by Lic-Orthion. 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 1986-06-19.
- Submission: K862022
- Applicant / Sponsor: Lic-Orthion
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5880
- Decision date: 1986-06-19
Classification & Regulation
This clearance is catalogued under FDA product code JFB and 21 CFR 890.5880, within the Physical Medicine review panel as a Class II device.