K-number	K082043
Device name	CARRIAZO-PENDULAR MICROKERATOME
Applicant	Schwind Eye-Tech-Solutions GmbH & Co. KG
Product code	HNO
Device class	Class I
Decision date	Aug 1, 2008
Decision	Substantially Equivalent
Regulation	886.4370

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View the full FDA submission: accessdata.fda.gov

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CARRIAZO-PENDULAR MICROKERATOME

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