3M Littmann Electronic Stethoscope, Model 4100
FDA 510(k) K051790 · 3M Company
510(k) numberK051790
Submission
- Device name
- 3M Littmann Electronic Stethoscope, Model 4100
- Applicant
- 3M Company
St. Paul, MN, US - Received
- July 1, 2005
- Decision date
- July 25, 2005
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 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 Electronic Stethoscope, Model 4100 cleared by the FDA?
3M Littmann Electronic Stethoscope, Model 4100 (K051790) received a 510(k) decision of Substantially Equivalent on July 25, 2005, 24 days after the submission was received.
What is the product code of K051790?
The FDA product code is DQD – Stethoscope, Electronic, a Class II (moderate risk) device regulated under 21 CFR 870.1875.