510(k) · Radiology

DELTAVIEW MODEL 2.1

by RIVERAIN MEDICAL GROUP,LLC

DELTAVIEW MODEL 2.1 is an AI-enabled medical device from RIVERAIN MEDICAL GROUP,LLC that the U.S. FDA cleared through 510(k) K111776 on December 28, 2011. Its lead review panel is Radiology and its primary product code is LLZ (System, Image Processing, Radiological).

See also top radiology AI devices.

Key facts

Submission numberK111776
Pathway510(k)
Date of final decision
Company (FDA list)RIVERAIN MEDICAL GROUP,LLC
Lead review panelRadiology
Primary product codeLLZ — System, Image Processing, Radiological
Applicant (openFDA)Riverain Medical Group,Llc
Applicant locationMiamisburg, OH, US
Device classClass 2
Regulation number21 CFR 892.2050
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. DELTAVIEW MODEL 2.1 went through this pathway (K111776).

openFDA lists it as a Class 2 device under 21 CFR 892.2050. Class II devices are moderate risk and are subject to general and special controls.

Product code LLZ covers 161 devices on the FDA AI list. By decision date, this device is #2 of 161 under that code. RIVERAIN MEDICAL GROUP,LLC has 1 AI-enabled device 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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