510(k) K250233

Device
PreemptiveAI Clinical SDK
Applicant
Measure Labs, Inc. (Dba Preemptiveai, Inc.)
510(k) number
K250233
Product code
DXH
Decision
Substantially Equivalent (SESE)
Decision date
2026-02-13
Date received
2025-01-27
Regulation
870.2920
Classification name
Transmitters And Receivers, Electrocardiograph, Telephone
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Matt Whitehill
Address
2101 N 34th St. Suite 195 Seattle WA US 98103 98103

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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