meddevicedb.com FDA Device Reference

CFR QUANT

K113754 Class II Traditional
Decision Date
2012-07-19
Sponsor / Applicant
University of Texas Medical School AT Houston

Technical Specification

510(k) Submission ID K113754
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 2012-07-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CFR QUANT received FDA 510(k) clearance under submission number K113754, sponsored by University of Texas Medical School AT Houston. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2012-07-19.

Classification & Regulation

This clearance is catalogued under FDA product code KPS and 21 CFR 892.1200, within the Radiology review panel as a Class II device.