FDA 510(k) FDA class 2 Substantially Equivalent 🇵🇱 Poland

DeepRhythmAI

K Number: K253141 · Decision Dec 11, 2025
Classifications
1
FEI Numbers
178
Registration Numbers
178
Same Product Code
429
Applicant Total
11
Review Days
77

Basic Information

Device Name
DeepRhythmAI
K Number
K253141
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1425
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicalgorithmics S.A.
Date Received
September 25, 2025
Decision Date
December 11, 2025
Product Code
DQK
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DQK Computer, Diagnostic, Programmable

Similar 510(k) Clearances

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Other Clearances by Medicalgorithmics S.A.

K Number Device Name
K250932 DeepRhythmAI
K241197 DeepRhythmAI
K232161 DeepRhythm Platform
K210822 DeepRhythmAI
K210758 Q Patch
K193104 Unified Arrhythmia Diagnostic System PocketECG IV
K173969 Medicalgorithmics Unified Cardiac Rehabilitation System
K152550 MEDICALGORITHMICS UNIFIED ARRHYTHMIA DIAGNOSIC SYSTEM
K124060 MEDICAL GORITHMICS UNIFIED ARRHYTHMIA DIAGNOSTIC SYSTEM
K112921 MEDICALGORITHMICS UNIFIED ARRHYTHMIA DIAGNOSTIC SYSTEM
Search all 11 clearances from Medicalgorithmics S.A. →