AccurSound Electronic Stethoscope AS-101

FDA 510(k) K221805 · Heroic Faith International , Ltd.

Substantially Equivalent

510(k) numberK221805

Submission

Device name
AccurSound Electronic Stethoscope AS-101
Applicant
Heroic Faith International , Ltd.
Taipei City, TW
Received
June 22, 2022
Decision date
March 23, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DQD – Stethoscope, Electronic
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1875
Specialty
Cardiovascular

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K251494Eko Foundation Analysis Software with Transformers (EFAST)DQD · Traditional Eko Health, Inc.08/12/2025SE
K242971AccurSound Electronic Stethoscope (AS101)DQD · Traditional Heroic Faith International , Ltd.11/25/2024SE
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More from Sparrow Acoustics, Inc.

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Questions and answers

When was AccurSound Electronic Stethoscope AS-101 cleared by the FDA?

AccurSound Electronic Stethoscope AS-101 (K221805) received a 510(k) decision of Substantially Equivalent on March 23, 2023, 274 days after the submission was received.

What is the product code of K221805?

The FDA product code is DQD – Stethoscope, Electronic, a Class II (moderate risk) device regulated under 21 CFR 870.1875.