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FDA 510(k)

ELECTRONIC-AMPLIFIED STETHOSCOPE

K-Number: K941763 · 1994-09-06

ApplicantHsues' Brothers Medical, Inc.
Decision Date1994-09-06
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC-AMPLIFIED STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Hsues' Brothers Medical, Inc.. It received FDA 510(k) clearance on 1994-09-06 under 510(k) number K941763. 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 ELECTRONIC-AMPLIFIED STETHOSCOPE?

ELECTRONIC-AMPLIFIED STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1994-09-06. The listed applicant is Hsues' Brothers Medical, Inc.. The 510(k) number is K941763.

When did ELECTRONIC-AMPLIFIED STETHOSCOPE receive FDA 510(k) clearance?

ELECTRONIC-AMPLIFIED STETHOSCOPE received FDA 510(k) clearance on 1994-09-06, under 510(k) number K941763.

Who is the listed applicant for ELECTRONIC-AMPLIFIED STETHOSCOPE?

The FDA 510(k) record lists Hsues' Brothers Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRONIC-AMPLIFIED STETHOSCOPE?

The FDA product code for ELECTRONIC-AMPLIFIED STETHOSCOPE is DQD.

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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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