K-number	K082278
Device name	MAMMOMARK, MAMMOMARK MR AND CORMARK BIOPSY SITE IDENTIFIERS
Applicant	Ethicon Endo-Sugery, LLC
Product code	NEU
Device class	Class II
Decision date	Dec 16, 2008
Decision	Substantially Equivalent
Regulation	878.4300

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View the full FDA submission: accessdata.fda.gov

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MAMMOMARK, MAMMOMARK MR AND CORMARK BIOPSY SITE IDENTIFIERS

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