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FDA 510(k)

Q Patch

K-Number: K210758 · 2022-06-02

Decision Date2022-06-02
Product CodeMWJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Q Patch is a medical device manufactured by Medicalgorithmics S.A.. It received FDA 510(k) clearance on 2022-06-02 under approval number K210758. The device is classified under product code MWJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Q Patch?

Q Patch is a medical device that received FDA 510(k) clearance on 2022-06-02. It is manufactured by Medicalgorithmics S.A.. The 510(k) number is K210758.

When was Q Patch approved by the FDA?

Q Patch received FDA 510(k) clearance on 2022-06-02, under approval number K210758.

What company makes Q Patch?

Q Patch is manufactured by Medicalgorithmics S.A..

What is the FDA product code for Q Patch?

The FDA product code for Q Patch is MWJ.

Other Devices by Medicalgorithmics S.A.

View all 8 devices →

Related Devices (Code: MWJ)

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.