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FDA 510(k)

LABTRON ELECTROMAX ELECTRONIC STETHOSCOPE MODEL NO. 04-1060

K-Number: K961857 · 1996-07-03

ApplicantGraham-Field, Inc.
Decision Date1996-07-03
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LABTRON ELECTROMAX ELECTRONIC STETHOSCOPE MODEL NO. 04-1060 is the device name listed in this FDA 510(k) record. The listed applicant is Graham-Field, Inc.. It received FDA 510(k) clearance on 1996-07-03 under 510(k) number K961857. 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 LABTRON ELECTROMAX ELECTRONIC STETHOSCOPE MODEL NO. 04-1060?

LABTRON ELECTROMAX ELECTRONIC STETHOSCOPE MODEL NO. 04-1060 is a medical device that received FDA 510(k) clearance on 1996-07-03. The listed applicant is Graham-Field, Inc.. The 510(k) number is K961857.

When did LABTRON ELECTROMAX ELECTRONIC STETHOSCOPE MODEL NO. 04-1060 receive FDA 510(k) clearance?

LABTRON ELECTROMAX ELECTRONIC STETHOSCOPE MODEL NO. 04-1060 received FDA 510(k) clearance on 1996-07-03, under 510(k) number K961857.

Who is the listed applicant for LABTRON ELECTROMAX ELECTRONIC STETHOSCOPE MODEL NO. 04-1060?

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

What is the FDA product code for LABTRON ELECTROMAX ELECTRONIC STETHOSCOPE MODEL NO. 04-1060?

The FDA product code for LABTRON ELECTROMAX ELECTRONIC STETHOSCOPE MODEL NO. 04-1060 is DQD.

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Other records listing Graham-Field, Inc. as applicant

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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