510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K250233Substantially Equivalent

PreemptiveAI Clinical SDK

Measure Labs, Inc. (dba Preemptiveai, Inc.), Seattle WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K250233 is the FDA 510(k) clearance record for PreemptiveAI Clinical SDK, a class II device, cleared for Measure Labs, Inc. (Dba Preemptiveai, Inc.) on under FDA product code DXH (Transmitters And Receivers, Electrocardiograph, Telephone). FDA records list one 510(k) clearance for Measure Labs, Inc. (Dba Preemptiveai, Inc.). As of , FDA records show no recalls naming K250233.

Clearance record

Decision date
Received
(382 days to decision)
Product code
DXH Transmitters And Receivers, Electrocardiograph, Telephone
Regulation
21 CFR 870.2920
Device class
Class II
Review panel
Cardiovascular
Applicant
Measure Labs, Inc. (Dba Preemptiveai, Inc.) 2101 N 34th St., Seattle WA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DXH

Trailing 12 months
4 clearances under product code DXH in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code DXH, trailing twelve months
MonthClearances
November 20251
December 20252
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260