K-number	K032217
Device name	14G CORMARK BIOPSY SITE IDENTIFIER
Applicant	Artemis Medical, Inc.
Product code	FZP
Device class	Class II
Decision date	Aug 21, 2003
Decision	Substantially Equivalent
Regulation	878.4300

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View the full FDA submission: accessdata.fda.gov

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14G CORMARK BIOPSY SITE IDENTIFIER

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