K-number	K802171
Device name	KODAK ORTHO L FILM
Applicant	Eastman Kodak Company
Product code	IWZ
Device class	Class I
Decision date	Oct 31, 1980
Decision	Substantially Equivalent
Regulation	892.1840

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View the full FDA submission: accessdata.fda.gov

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KODAK ORTHO L FILM

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