Devices · Tempus AI, Inc.

Tempus ECG-Low EF

Tempus AI, Inc. is listed for Tempus ECG-Low EF (K250119). The FDA list gives July 15, 2025 as the date of the final decision. The lead panel is Cardiovascular, and the database link on the FDA list is the 510(k) pathway. openFDA describes product code QYE as “Reduced Ejection Fraction Machine Learning-Based Notification Software”: Reduced Ejection Fraction machine learning-based notification software employs machine learning techniques to suggest the likelihood of a reduced ejection fraction for further referral or diagnostic follow-up. openFDA records this submission’s decision description as “Substantially Equivalent.” This paragraph is assembled only from those public fields. It is not an FDA review, not a determination of safety or effectiveness, and not medical advice. Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K250119

Official FDA database record

Date of final decision

July 15, 2025

Company on the FDA list

Tempus AI, Inc.

Lead panel

Cardiovascular

Primary product code

QYE

openFDA device name for the code

Reduced Ejection Fraction Machine Learning-Based Notification Software

Device class

2

Regulation number

870.2380

openFDA decision description

Substantially Equivalent

openFDA decision code

SESE

Statement or summary label

Summary