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FDA 510(k)

CardioLogs ECG Analysis Platform

K-Number: K170568 · 2017-06-26

ApplicantCardiologs Technologies
Decision Date2017-06-26
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CardioLogs ECG Analysis Platform is a medical device manufactured by Cardiologs Technologies. It received FDA 510(k) clearance on 2017-06-26 under approval number K170568. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CardioLogs ECG Analysis Platform?

CardioLogs ECG Analysis Platform is a medical device that received FDA 510(k) clearance on 2017-06-26. It is manufactured by Cardiologs Technologies. The 510(k) number is K170568.

When was CardioLogs ECG Analysis Platform approved by the FDA?

CardioLogs ECG Analysis Platform received FDA 510(k) clearance on 2017-06-26, under approval number K170568.

What company makes CardioLogs ECG Analysis Platform?

CardioLogs ECG Analysis Platform is manufactured by Cardiologs Technologies.

What is the FDA product code for CardioLogs ECG Analysis Platform?

The FDA product code for CardioLogs ECG Analysis Platform is DPS.

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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.

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