Clearance Summary
L-SER KO LAMP received FDA 510(k) clearance under submission number K112016, sponsored by Ya-Man, 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 2012-02-10.
- Submission: K112016
- Applicant / Sponsor: Ya-Man, Ltd.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5500
- Decision date: 2012-02-10
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.