meddevicedb.com FDA Device Reference

1125 XSB XENON FIBER-OPTIC LIGHT SOURCE

K052979 Class II Traditional
Decision Date
2005-10-31
Sponsor / Applicant
Isolux, LLC

Technical Specification

510(k) Submission ID K052979
Product Code HBI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4580
Decision Date 2005-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

1125 XSB XENON FIBER-OPTIC LIGHT SOURCE received FDA 510(k) clearance under submission number K052979, sponsored by Isolux, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2005-10-31.

Classification & Regulation

This clearance is catalogued under FDA product code HBI and 21 CFR 878.4580, within the General, Plastic Surgery review panel as a Class II device.