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FDA 510(k)

3M LITTMANN GRAPHIC DISPLAY SYSTEM

K-Number: K920009 · 1992-10-21

Applicant3M Health Care, Ltd.
Decision Date1992-10-21
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

3M LITTMANN GRAPHIC DISPLAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is 3M Health Care, Ltd.. It received FDA 510(k) clearance on 1992-10-21 under 510(k) number K920009. 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 GRAPHIC DISPLAY SYSTEM?

3M LITTMANN GRAPHIC DISPLAY SYSTEM is a medical device that received FDA 510(k) clearance on 1992-10-21. The listed applicant is 3M Health Care, Ltd.. The 510(k) number is K920009.

When did 3M LITTMANN GRAPHIC DISPLAY SYSTEM receive FDA 510(k) clearance?

3M LITTMANN GRAPHIC DISPLAY SYSTEM received FDA 510(k) clearance on 1992-10-21, under 510(k) number K920009.

Who is the listed applicant for 3M LITTMANN GRAPHIC DISPLAY SYSTEM?

The FDA 510(k) record lists 3M Health Care, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M LITTMANN GRAPHIC DISPLAY SYSTEM?

The FDA product code for 3M LITTMANN GRAPHIC DISPLAY SYSTEM is DQD.

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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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