K-number	K123316
Device name	HEINE OMEGA 500
Applicant	Heine Optotechnik GmbH & Co. KG
Product code	HLI
Device class	Class II
Decision date	Feb 26, 2013
Decision	Substantially Equivalent
Regulation	886.1570

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View the full FDA submission: accessdata.fda.gov

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HEINE OMEGA 500

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