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FDA 510(k)

MyHomeDoc

K-Number: K202483 · 2021-03-23

ApplicantMyhomedoc , Ltd.
Decision Date2021-03-23
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MyHomeDoc is the device name listed in this FDA 510(k) record. The listed applicant is Myhomedoc , Ltd.. It received FDA 510(k) clearance on 2021-03-23 under 510(k) number K202483. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MyHomeDoc?

MyHomeDoc is a medical device that received FDA 510(k) clearance on 2021-03-23. The listed applicant is Myhomedoc , Ltd.. The 510(k) number is K202483.

When did MyHomeDoc receive FDA 510(k) clearance?

MyHomeDoc received FDA 510(k) clearance on 2021-03-23, under 510(k) number K202483.

Who is the listed applicant for MyHomeDoc?

The FDA 510(k) record lists Myhomedoc , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MyHomeDoc?

The FDA product code for MyHomeDoc is DQD.

Related Clinical Trials

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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