510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K083903Substantially Equivalent

3M Littmann Electronic Stethoscope, Model 3200

3M Company, St. Paul MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K083903 is the FDA 510(k) clearance record for 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3200, a class II device, cleared for 3M Company on under FDA product code DQD (Stethoscope, Electronic). FDA records list 146 510(k) clearances for 3M Company, from to . As of , FDA records show no recalls naming K083903.

Clearance record

Decision date
Received
(198 days to decision)
Product code
DQD Stethoscope, Electronic
Regulation
21 CFR 870.1875
Device class
Class II
Review panel
Cardiovascular
Applicant
3M Company 3m Center, Bldg. 275-5w-06, St. Paul MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DQD

Trailing 12 months
7 clearances under product code DQD in the twelve months to November 2026, July 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code DQD, trailing twelve months
MonthClearances
December 20251
January 20260
February 20261
March 20261
April 20260
May 20261
June 20260
July 20262
August 20260
September 20260
October 20261
November 20260