K-number	K932357
Device name	FUJI EC ID CAMERA
Applicant	Fujifilm Medical System U.S.A., Inc.
Product code	JAC
Device class	Class I
Decision date	Jul 26, 1993
Decision	Substantially Equivalent
Regulation	892.1640

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View the full FDA submission: accessdata.fda.gov

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FUJI EC ID CAMERA

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