K-number	K131961
Device name	HEINE BETA 200(R) OPHTHALMOSCOPE
Applicant	Heine Optotechnik GmbH & Co. KG
Product code	HLJ
Device class	Class II
Decision date	Dec 4, 2013
Decision	Substantially Equivalent
Regulation	886.1570

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View the full FDA submission: accessdata.fda.gov

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HEINE BETA 200(R) OPHTHALMOSCOPE

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