meddevicedb.com FDA Device Reference

DOSIMETRY CHECK

K010225 Class II Traditional
Decision Date
2001-04-24
Sponsor / Applicant
Math Resolutions, LLC

Technical Specification

510(k) Submission ID K010225
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2001-04-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DOSIMETRY CHECK received FDA 510(k) clearance under submission number K010225, 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 2001-04-24.

Classification & Regulation

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