3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3200
K-Number: K083903 · 2009-07-15
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Device Summary
Frequently Asked Questions
What is the 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3200?
3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3200 is a medical device that received FDA 510(k) clearance on 2009-07-15. The listed applicant is 3M Company. The 510(k) number is K083903.
When did 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3200 receive FDA 510(k) clearance?
3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3200 received FDA 510(k) clearance on 2009-07-15, under 510(k) number K083903.
Who is the listed applicant for 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3200?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3200?
The FDA product code for 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3200 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.
Other records listing 3M Company 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.
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.
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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