K-number	K893992
Device name	NOETIX, BIOPSY NEEDLE
Applicant	Noetix, Inc.
Product code	KNW
Device class	Class II
Decision date	Sep 8, 1989
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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NOETIX, BIOPSY NEEDLE

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