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510(k) clearance

Kinetic Software Library

FDA 510(k) source

510(k) number
K260640
Applicant
Monebo Technologies, Inc.
Decision date
Oct 23, 2026
Date received
Feb 27, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
DPS
Device type
Electrocardiograph
Device class
Class II
Regulation
21 CFR 870.2340
Advisory committee
Cardiovascular
Statement or summary
Summary
Third party
N
Location
Austin, TX, US