meddevicedb.com FDA Device Reference

XENON-100 SCB LIGHT SOURCE, MODEL 20132620

K082925 Class II Traditional
Decision Date
2008-12-18
Sponsor / Applicant
KARL STORZ Endoscopy-America, Inc.

Technical Specification

510(k) Submission ID K082925
Product Code GCT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2008-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

XENON-100 SCB LIGHT SOURCE, MODEL 20132620 received FDA 510(k) clearance under submission number K082925, sponsored by KARL STORZ Endoscopy-America, 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 2008-12-18.

Classification & Regulation

This clearance is catalogued under FDA product code GCT and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.