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FDA 510(k)

Q Patch

K-Number: K210758 · 2022-06-02

ApplicantMedicalgorithmics S.A.
Decision Date2022-06-02
Product CodeMWJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Q Patch is the device name listed in this FDA 510(k) record. The listed applicant is Medicalgorithmics S.A.. It received FDA 510(k) clearance on 2022-06-02 under 510(k) 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. The listed applicant is Medicalgorithmics S.A.. The 510(k) number is K210758.

When did Q Patch receive FDA 510(k) clearance?

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

Who is the listed applicant for Q Patch?

The FDA 510(k) record lists Medicalgorithmics S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Q Patch?

The FDA product code for Q Patch is MWJ.

Other records listing Medicalgorithmics S.A. as applicant

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Related Devices (Code: MWJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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