510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K120704Substantially Equivalent

3M Littmann Telesteth Online Ausculation System

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

K120704 is the FDA 510(k) clearance record for 3M LITTMANN TELESTETH ONLINE AUSCULATION SYSTEM, a class II device, cleared for 3M Company on under FDA product code DRG (Transmitters And Receivers, Physiological Signal, Radiofrequency). FDA records list 146 510(k) clearances for 3M Company, from to . As of , FDA records show no recalls naming K120704.

Clearance record

Decision date
Received
(56 days to decision)
Product code
DRG Transmitters And Receivers, Physiological Signal, Radiofrequency
Regulation
21 CFR 870.2910
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 DRG

Trailing 12 months
2 clearances under product code DRG in the twelve months to November 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DRG, trailing twelve months
MonthClearances
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260
November 20260