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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Sound Land Corp.. It received FDA 510(k) clearance on 2022-11-03 under 510(k) 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. The listed applicant is Sound Land Corp.. The 510(k) number is K220466.

When did ibiomedi Electronic Stethoscope ES-2020 receive FDA 510(k) clearance?

ibiomedi Electronic Stethoscope ES-2020 received FDA 510(k) clearance on 2022-11-03, under 510(k) number K220466.

Who is the listed applicant for ibiomedi Electronic Stethoscope ES-2020?

The FDA 510(k) record lists Sound Land Corp. as the applicant. This does not by itself establish the device manufacturer.

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 Devices (Code: DQD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261494Smart Wireless Stethoscope (STEMO310);Smart Wireless Stethoscope (STEMO710);Smart Wireless Stethoscope (STEMO720);Smart Wireless Stethoscope (STEMO730)Shanghai Hulu Devices Co., Ltd.K261694CORE 300 Digital StethoscopeEko Health, Inc.K252915AiSteth®Ai Health Highway India Pvt., Ltd.K252089Tyto Stethoscope (G3)Tyto Care , Ltd.K252076Kneevoice Cartilage Evaluation System (750-3600-001)Kneevoice, Inc.K252284eMurmur Heart AICsd Labs

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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