K-number	K021640
Device name	HANSATOME EXCELLUS MICROKERATOME
Applicant	Bausch & Lomb, Inc.
Product code	HNO
Device class	Class I
Decision date	Jun 19, 2002
Decision	Substantially Equivalent
Regulation	886.4370

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View the full FDA submission: accessdata.fda.gov

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HANSATOME EXCELLUS MICROKERATOME

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