DeepRhythmAI
K-Number: K210822 · 2022-07-27
ApplicantMedicalgorithmics S.A.
Decision Date2022-07-27
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
DeepRhythmAI is a medical device manufactured by Medicalgorithmics S.A.. It received FDA 510(k) clearance on 2022-07-27 under approval number K210822. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the DeepRhythmAI?
DeepRhythmAI is a medical device that received FDA 510(k) clearance on 2022-07-27. It is manufactured by Medicalgorithmics S.A.. The 510(k) number is K210822.
When was DeepRhythmAI approved by the FDA?
DeepRhythmAI received FDA 510(k) clearance on 2022-07-27, under approval number K210822.
What company makes DeepRhythmAI?
DeepRhythmAI is manufactured by Medicalgorithmics S.A..
What is the FDA product code for DeepRhythmAI?
The FDA product code for DeepRhythmAI is DQK.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.