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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Processor, Cine Film
510(k) Number K913241
Device Name JAMIESON JT-CRP CINE FILM PROCESSOR
Applicant
Jamieson Film Co.
10425 Olympic Dr.
Dallas,  TX  75220
Applicant Contact GARY FULLER
Correspondent
Jamieson Film Co.
10425 Olympic Dr.
Dallas,  TX  75220
Correspondent Contact GARY FULLER
Regulation Number892.1900
Classification Product Code
IXX  
Date Received07/22/1991
Decision Date 09/24/1991
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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