K-number	K023092
Device name	BD K-4000 MICROKERATOME SYSTEM
Applicant	Becton, Dickinson & CO
Product code	HMY
Device class	Class I
Decision date	Oct 18, 2002
Decision	Substantially Equivalent
Regulation	886.4370

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View the full FDA submission: accessdata.fda.gov

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BD K-4000 MICROKERATOME SYSTEM

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