3M Littmann Graphic Display System
FDA 510(k) K920009 · 3M Health Care, Ltd.
510(k) numberK920009
Submission
- Device name
- 3M Littmann Graphic Display System
- Applicant
- 3M Health Care, Ltd.
St. Paul, MN, US - Received
- January 2, 1992
- Decision date
- October 21, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DQD – Stethoscope, Electronic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1875
- Specialty
- Cardiovascular
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Questions and answers
When was 3M Littmann Graphic Display System cleared by the FDA?
3M Littmann Graphic Display System (K920009) received a 510(k) decision of Substantially Equivalent on October 21, 1992, 293 days after the submission was received.
What is the product code of K920009?
The FDA product code is DQD – Stethoscope, Electronic, a Class II (moderate risk) device regulated under 21 CFR 870.1875.