K-number	K943821
Device name	KYOKKO SPEC-SERIES INTENSIFY SCREENS-SPEC,SUPER SPEC
Applicant	Fujifilm Medical System U.S.A., Inc.
Product code	EAM
Device class	Class I
Decision date	Aug 22, 1994
Decision	Substantially Equivalent
Regulation	892.1960

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KYOKKO SPEC-SERIES INTENSIFY SCREENS-SPEC,SUPER SPEC

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