MyHomeDoc— 510(k) K202483

Substantially Equivalent

Myhomedoc , Ltd.

FDA 510(k) clearance K202483 for MyHomeDoc, Substantially Equivalent on 2021-03-23. Applicant: Myhomedoc , Ltd..

Clearance details

Applicant: Myhomedoc , Ltd.
Product code: Code DQD
Advisory panel: Cardiovascular
Date received: 2020-08-28
Decision date: 2021-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ra'Anana, IL

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