K-number	K964414
Device name	LR 5200 LASER FILM RECORDER
Applicant	Bayer Corp., Agfa Div.
Product code	LMC
Device class	Class II
Decision date	Jan 27, 1997
Decision	Substantially Equivalent
Regulation	892.2040

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View the full FDA submission: accessdata.fda.gov

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LR 5200 LASER FILM RECORDER

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