meddevicedb.com FDA Device Reference

ART BRACHYTHERAPY APPLICATOR

K060299 Class II Traditional
Decision Date
2006-06-06
Sponsor / Applicant
Advanced Radiation Therapy, LLC

Technical Specification

510(k) Submission ID K060299
Product Code JAQ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5700
Decision Date 2006-06-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ART BRACHYTHERAPY APPLICATOR received FDA 510(k) clearance under submission number K060299, sponsored by Advanced Radiation Therapy, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2006-06-06.

Classification & Regulation

This clearance is catalogued under FDA product code JAQ and 21 CFR 892.5700, within the Radiology review panel as a Class II device.