Clearance Summary
XENON ARC ENDOSCOPE LIGHT SOURCE received FDA 510(k) clearance under submission number K920403, sponsored by Medical Device Inspection Co., 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 1992-02-21.
- Submission: K920403
- Applicant / Sponsor: Medical Device Inspection Co., Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 1992-02-21
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.