FDA 510(k) Application Details - K963334

Device Classification Name	Processor, Cine Film   More FDA Info for this Device
510(K) Number	K963334
Device Name	Processor, Cine Film
Applicant	JAMIESON FILM CO. 10425 OLYMPIC DR. DALLAS, TX 75220-4427 US Other 510(k) Applications for this Company
Contact	GEORGE LEON Other 510(k) Applications for this Contact
Regulation Number	892.1900   More FDA Info for this Regulation Number
Classification Product Code	IXX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/26/1996
Decision Date	09/11/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review