K-number	K951307
Device name	BAXTER TREK *14 INTERMEDIATE AND SUPPORT GUIDEWIRES
Applicant	Baxter Healthcare Corp
Product code	DQX
Device class	Class II
Decision date	Jun 22, 1995
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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BAXTER TREK *14 INTERMEDIATE AND SUPPORT GUIDEWIRES

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