meddevicedb.com FDA Device Reference

DeepRhythmAI

K210822 Class II Traditional
Decision Date
2022-07-27
Sponsor / Applicant
Medicalgorithmics S.A.

Technical Specification

510(k) Submission ID K210822
Product Code DQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1425
Decision Date 2022-07-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DeepRhythmAI received FDA 510(k) clearance under submission number K210822, sponsored by Medicalgorithmics S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2022-07-27.

Classification & Regulation

This clearance is catalogued under FDA product code DQK and 21 CFR 870.1425, within the Cardiovascular review panel as a Class II device.