K-number	K001144
Device name	ULTRAEDGE KERATOME BLADE, MODEL 374803 - ACS
Applicant	Lasersight Technologies, Inc.
Product code	HNO
Device class	Class I
Decision date	May 5, 2000
Decision	Substantially Equivalent
Regulation	886.4370

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View the full FDA submission: accessdata.fda.gov

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ULTRAEDGE KERATOME BLADE, MODEL 374803 - ACS

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