MyHomeDoc
K-Number: K202483 · 2021-03-23
ApplicantMyhomedoc , Ltd.
Decision Date2021-03-23
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
MyHomeDoc is a medical device manufactured by Myhomedoc , Ltd.. It received FDA 510(k) clearance on 2021-03-23 under approval 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. It is manufactured by Myhomedoc , Ltd.. The 510(k) number is K202483.
When was MyHomeDoc approved by the FDA?
MyHomeDoc received FDA 510(k) clearance on 2021-03-23, under approval number K202483.
What company makes MyHomeDoc?
MyHomeDoc is manufactured by Myhomedoc , Ltd..
What is the FDA product code for MyHomeDoc?
The FDA product code for MyHomeDoc is DQD.
Related Devices (Code: DQD)
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.