ibiomedi Electronic Stethoscope ES-2020
K-Number: K220466 · 2022-11-03
ApplicantSound Land Corp.
Decision Date2022-11-03
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
ibiomedi Electronic Stethoscope ES-2020 is a medical device manufactured by Sound Land Corp.. It received FDA 510(k) clearance on 2022-11-03 under approval number K220466. 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 ibiomedi Electronic Stethoscope ES-2020?
ibiomedi Electronic Stethoscope ES-2020 is a medical device that received FDA 510(k) clearance on 2022-11-03. It is manufactured by Sound Land Corp.. The 510(k) number is K220466.
When was ibiomedi Electronic Stethoscope ES-2020 approved by the FDA?
ibiomedi Electronic Stethoscope ES-2020 received FDA 510(k) clearance on 2022-11-03, under approval number K220466.
What company makes ibiomedi Electronic Stethoscope ES-2020?
ibiomedi Electronic Stethoscope ES-2020 is manufactured by Sound Land Corp..
What is the FDA product code for ibiomedi Electronic Stethoscope ES-2020?
The FDA product code for ibiomedi Electronic Stethoscope ES-2020 is DQD.
Related Clinical Trials
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.