K-number	K890203
Device name	ADMS BIOPSY NEEDLE
Applicant	Advanced Diagnostic Medical Systems, Inc.
Product code	FCG
Device class	Class II
Decision date	Mar 8, 1989
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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ADMS BIOPSY NEEDLE

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