K-number	K953887
Device name	RE-USABLE CONCENTRIC NEEDLE
Applicant	Chalgren Enterprises, Inc.
Product code	IKT
Device class	Class II
Decision date	Oct 31, 1995
Decision	Substantially Equivalent
Regulation	890.1385

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View the full FDA submission: accessdata.fda.gov

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RE-USABLE CONCENTRIC NEEDLE

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