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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Camera, Multi Format, Radiological
510(k) Number K936152
Device Name 3M 1152 LASER IMAGER
Applicant
3M Information,Imaging and Electronic Sector
3m Center, Bldg. 235-2b-23
St. Paul,  MN  55144
Applicant Contact WARREN L SNYDER
Correspondent
3M Information,Imaging and Electronic Sector
3m Center, Bldg. 235-2b-23
St. Paul,  MN  55144
Correspondent Contact WARREN L SNYDER
Regulation Number892.2040
Classification Product Code
LMC  
Date Received12/27/1993
Decision Date 09/21/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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