eClinic Stethopod
K-Number: K220099 · 2022-10-20
ApplicantHomediagnostic, LLC
Decision Date2022-10-20
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
eClinic Stethopod is a medical device manufactured by Homediagnostic, LLC. It received FDA 510(k) clearance on 2022-10-20 under approval number K220099. 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 eClinic Stethopod?
eClinic Stethopod is a medical device that received FDA 510(k) clearance on 2022-10-20. It is manufactured by Homediagnostic, LLC. The 510(k) number is K220099.
When was eClinic Stethopod approved by the FDA?
eClinic Stethopod received FDA 510(k) clearance on 2022-10-20, under approval number K220099.
What company makes eClinic Stethopod?
eClinic Stethopod is manufactured by Homediagnostic, LLC.
What is the FDA product code for eClinic Stethopod?
The FDA product code for eClinic Stethopod 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.