K-number	K043222
Device name	VISCUCAM C DIGITAL CAMERA
Applicant	Carl Zeiss Meditec, AG
Product code	HKI
Device class	Class II
Decision date	Feb 14, 2005
Decision	Substantially Equivalent
Regulation	886.1120

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View the full FDA submission: accessdata.fda.gov

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VISCUCAM C DIGITAL CAMERA

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