K-number	K102768
Device name	SECRMARK BIOPSY SITE MARKING SYSTEM
Applicant	Hologic, Inc.
Product code	NEU
Device class	Class II
Decision date	Dec 2, 2010
Decision	Substantially Equivalent
Regulation	878.4300

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View the full FDA submission: accessdata.fda.gov

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SECRMARK BIOPSY SITE MARKING SYSTEM

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