meddevicedb.com FDA Device Reference

DOSE VOLUME HISTOGRAM (DVH) EVALUATOR

K092928 Class II Traditional
Decision Date
2009-12-16
Sponsor / Applicant
Diversilabs, LLC

Technical Specification

510(k) Submission ID K092928
Product Code MUJ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2009-12-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DOSE VOLUME HISTOGRAM (DVH) EVALUATOR received FDA 510(k) clearance under submission number K092928, sponsored by Diversilabs, 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 2009-12-16.

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.