K-number	K020482
Device name	KERATOME BLADE 200200 & 600600
Applicant	Micro Specialties, Inc.
Product code	HNO
Device class	Class I
Decision date	Dec 16, 2002
Decision	Substantially Equivalent
Regulation	886.4370

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View the full FDA submission: accessdata.fda.gov

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KERATOME BLADE 200200 & 600600

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