K-number	K834237
Device name	GRADUATED GUIDE WIRE BOWL 8
Applicant	Sterile Design, Inc.
Product code	DQX
Device class	Class II
Decision date	Feb 4, 1984
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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GRADUATED GUIDE WIRE BOWL 8

Everything you need for a 510(k) submission. Nothing you don't.