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FDA 510(k)

MEDITRON STETHOSCOPE SYSTEM

K-Number: K991367 · 1999-07-19

ApplicantMeditron AS
Decision Date1999-07-19
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDITRON STETHOSCOPE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Meditron AS. It received FDA 510(k) clearance on 1999-07-19 under 510(k) number K991367. 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 MEDITRON STETHOSCOPE SYSTEM?

MEDITRON STETHOSCOPE SYSTEM is a medical device that received FDA 510(k) clearance on 1999-07-19. The listed applicant is Meditron AS. The 510(k) number is K991367.

When did MEDITRON STETHOSCOPE SYSTEM receive FDA 510(k) clearance?

MEDITRON STETHOSCOPE SYSTEM received FDA 510(k) clearance on 1999-07-19, under 510(k) number K991367.

Who is the listed applicant for MEDITRON STETHOSCOPE SYSTEM?

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

What is the FDA product code for MEDITRON STETHOSCOPE SYSTEM?

The FDA product code for MEDITRON STETHOSCOPE SYSTEM is DQD.

Related Clinical Trials

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.

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Other records listing Meditron AS as applicant

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.

K013725MEDITRON II THESTERTHOSCOPE SYSTEM

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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