K-number	K022560
Device name	M2 SINGLE USE MICROKERTOME
Applicant	Moria SA
Product code	HMY
Device class	Class I
Decision date	Sep 27, 2002
Decision	Substantially Equivalent
Regulation	886.4370

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View the full FDA submission: accessdata.fda.gov

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M2 SINGLE USE MICROKERTOME

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