meddevicedb.com FDA Device Reference

RTDOSEPLAN

K022961 Class II Traditional
Decision Date
2003-01-31
Sponsor / Applicant
Math Resolutions, LLC

Technical Specification

510(k) Submission ID K022961
Product Code MUJ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2003-01-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RTDOSEPLAN received FDA 510(k) clearance under submission number K022961, sponsored by Math Resolutions, 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 2003-01-31.

Classification & Regulation

This clearance is catalogued under FDA product code MUJ and 21 CFR 892.5050, within the Radiology review panel as a Class II device.