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FDA 510(k)

RHYTHM DIGITAL ELECTRONIC STETHOSCOPE

K-Number: K032230 · 2003-11-26

ApplicantThinklabs, Inc.
Decision Date2003-11-26
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RHYTHM DIGITAL ELECTRONIC STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Thinklabs, Inc.. It received FDA 510(k) clearance on 2003-11-26 under 510(k) number K032230. 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 RHYTHM DIGITAL ELECTRONIC STETHOSCOPE?

RHYTHM DIGITAL ELECTRONIC STETHOSCOPE is a medical device that received FDA 510(k) clearance on 2003-11-26. The listed applicant is Thinklabs, Inc.. The 510(k) number is K032230.

When did RHYTHM DIGITAL ELECTRONIC STETHOSCOPE receive FDA 510(k) clearance?

RHYTHM DIGITAL ELECTRONIC STETHOSCOPE received FDA 510(k) clearance on 2003-11-26, under 510(k) number K032230.

Who is the listed applicant for RHYTHM DIGITAL ELECTRONIC STETHOSCOPE?

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

What is the FDA product code for RHYTHM DIGITAL ELECTRONIC STETHOSCOPE?

The FDA product code for RHYTHM DIGITAL ELECTRONIC 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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