K-number	K023450
Device name	BIOPSY SITE TISSUE MARKER DEVICE
Applicant	Promex, Inc.
Product code	NEU
Device class	Class II
Decision date	Dec 19, 2002
Decision	Substantially Equivalent
Regulation	878.4300

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View the full FDA submission: accessdata.fda.gov

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BIOPSY SITE TISSUE MARKER DEVICE

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