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FDA 510(k)

3M LITTMANN ELECTRONIC STETHOSCOPE

K-Number: K961848 · 1997-09-26

ApplicantMinnesota Mining and Mfg. Co.
Decision Date1997-09-26
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

3M LITTMANN ELECTRONIC STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Minnesota Mining and Mfg. Co.. It received FDA 510(k) clearance on 1997-09-26 under 510(k) number K961848. 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 3M LITTMANN ELECTRONIC STETHOSCOPE?

3M LITTMANN ELECTRONIC STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1997-09-26. The listed applicant is Minnesota Mining and Mfg. Co.. The 510(k) number is K961848.

When did 3M LITTMANN ELECTRONIC STETHOSCOPE receive FDA 510(k) clearance?

3M LITTMANN ELECTRONIC STETHOSCOPE received FDA 510(k) clearance on 1997-09-26, under 510(k) number K961848.

Who is the listed applicant for 3M LITTMANN ELECTRONIC STETHOSCOPE?

The FDA 510(k) record lists Minnesota Mining and Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M LITTMANN ELECTRONIC STETHOSCOPE?

The FDA product code for 3M LITTMANN ELECTRONIC STETHOSCOPE is DQD.

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Other records listing Minnesota Mining and Mfg. Co. 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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