Clearance Summary
SONY LMD-2451MT LCD MONITOR received FDA 510(k) clearance under submission number K113203, sponsored by Sony Electronics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2012-02-24.
- Submission: K113203
- Applicant / Sponsor: Sony Electronics, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2012-02-24
Classification & Regulation
This clearance is catalogued under FDA product code GCJ and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.