Critical Care Suite with Enteric Tube Positioning AI Algorithm

FDA 510(k) K253502 · Ge Medical Systems, LLC

Substantially Equivalent

510(k) numberK253502

Submission

Device name
Critical Care Suite with Enteric Tube Positioning AI Algorithm
Applicant
Ge Medical Systems, LLC
Waukesha, WI, US
Received
October 30, 2025
Decision date
April 14, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
QIH – Automated Radiological Image Processing Software
Device class
Class II (moderate risk)
Regulation
21 CFR 892.2050
Specialty
Radiology

To provide automated radiological image processing and analysis tools. Software implementing artificial intelligence including nonadaptive machine learning algorithms trained with clinical and/or artificial data. In these devices, the algorithm training data typically impacts device performance. Adaptive AI algorithms are not within scope of this product code.

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Questions and answers

When was Critical Care Suite with Enteric Tube Positioning AI Algorithm cleared by the FDA?

Critical Care Suite with Enteric Tube Positioning AI Algorithm (K253502) received a 510(k) decision of Substantially Equivalent on April 14, 2026, 166 days after the submission was received.

What is the product code of K253502?

The FDA product code is QIH – Automated Radiological Image Processing Software, a Class II (moderate risk) device regulated under 21 CFR 892.2050.