K-number	K990656
Device name	CHROMOPHARE D 530 LDR SURGICAL LIGHT
Applicant	Berchtold Holding GmbH
Product code	FSY
Device class	Class II
Decision date	Jul 20, 1999
Decision	Substantially Equivalent
Regulation	878.4580

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View the full FDA submission: accessdata.fda.gov

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CHROMOPHARE D 530 LDR SURGICAL LIGHT

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