510(k) · Radiology

qER

by Qure.ai Technologies

qER is an AI-enabled medical device from Qure.ai Technologies that the U.S. FDA cleared through 510(k) K200921 on June 17, 2020. Its lead review panel is Radiology and its primary product code is QAS (Radiological Computer-Assisted Triage And Notification Software).

See also FDA-cleared AI radiology devices in 2020, all FDA AI clearances in 2020, top radiology AI devices.

Key facts

Submission numberK200921
Pathway510(k)
Date of final decision
Company (FDA list)Qure.ai Technologies
Lead review panelRadiology
Primary product codeQAS — Radiological Computer-Assisted Triage And Notification Software
Applicant (openFDA)Qure.Ai Technologies
Applicant locationMumbai, IN
Device classClass 2
Regulation number21 CFR 892.2080
Decision codeSESE
Submission typeTraditional

Source: FDA AI-Enabled Medical Devices list and openFDA.

What this means

A 510(k) is a premarket submission showing the device is substantially equivalent to a legally marketed predicate device. A cleared 510(k) means FDA agreed with that equivalence. qER went through this pathway (K200921).

openFDA lists it as a Class 2 device under 21 CFR 892.2080. Class II devices are moderate risk and are subject to general and special controls.

Product code QAS covers 86 devices on the FDA AI list. By decision date, this device is #13 of 86 under that code. Qure.ai Technologies has 9 AI-enabled devices on the list, and the Radiology panel accounts for 1,230 in total.

Being on this list doesn't describe how well the device works clinically. Check the FDA record for its indications for use.

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