Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K936153Substantially Equivalent

3M 1156 Multi-Input System

3M Information,Imaging and Electronic Sector, St. Paul MN / Traditional, Substantially Equivalent

K936153 is the FDA 510(k) clearance record for 3M 1156 MULTI-INPUT SYSTEM, a class I device, cleared for 3M Information,Imaging and Electronic Sector on under FDA product code LMD (System, Digital Image Communications, Radiological). FDA's definition for product code LMD reads: "A medical image communications device provides electronic transfer of medical image data between medical devices. It may include a physical communications medium, modems, interfaces, and a communications protocol. It may provide simple...". FDA records list 3 510(k) clearances for 3M Information,Imaging and Electronic Sector, from to . As of , FDA records show no recalls naming K936153.

Clearance record

Decision date
Received
(147 days to decision)
Product code
LMD System, Digital Image Communications, Radiological
Regulation
21 CFR 892.2020
Device class
Class I
Review panel
Radiology
Applicant
3M Information,Imaging and Electronic Sector 3m Center, Bldg. 235-2b-23, St. Paul MN
510(k) summary
Summary
Third party review
No

Clearances, product code LMD

Trailing 12 months

FDA records hold no clearances under product code LMD in the trailing twelve months.

FDA records show no clearances under product code LMD in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LMD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260