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

DeepRhythm Platform

K Number: K232161 · Decision Jun 20, 2024
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
11
Review Days
336

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Basic Information

Device Name
DeepRhythm Platform
K Number
K232161
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicalgorithmics S.A.
Date Received
July 20, 2023
Decision Date
June 20, 2024
Product Code
DPS
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
DPS Electrocardiograph

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Other Clearances by Medicalgorithmics S.A.

K Number Device Name
K253141 DeepRhythmAI
K250932 DeepRhythmAI
K241197 DeepRhythmAI
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. →