K-number	K932700
Device name	CUTO(TM) TISSUE MORCELLATION SYSTEM
Applicant	Linvatec Corp.
Product code	GEY
Device class	Class I
Decision date	Oct 15, 1993
Decision	Substantially Equivalent
Regulation	878.4820

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View the full FDA submission: accessdata.fda.gov

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CUTO(TM) TISSUE MORCELLATION SYSTEM

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