meddevicedb.com FDA Device Reference

QLAB Advanced Quantification Software

K200974 Class II Traditional
Decision Date
2020-06-03
Sponsor / Applicant
Philips Health Care

Technical Specification

510(k) Submission ID K200974
Product Code QIH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2020-06-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QLAB Advanced Quantification Software received FDA 510(k) clearance under submission number K200974, sponsored by Philips Health Care. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2020-06-03.

Classification & Regulation

This clearance is catalogued under FDA product code QIH and 21 CFR 892.2050, within the Radiology review panel as a Class II device.