K-number	K173901
Device name	MyoSure MANUAL Tissue Removal Device
Applicant	Hologic, Inc.
Product code	HIH
Device class	Class II
Decision date	May 8, 2018
Decision	Substantially Equivalent
Regulation	884.1690

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Source

View the full FDA submission: accessdata.fda.gov

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MyoSure MANUAL Tissue Removal Device

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