K-number	K951109
Device name	C-THRU CORONARY GUIDE WIRE
Applicant	Schneider (Europe) GmbH
Product code	DQX
Device class	Class II
Decision date	Jun 8, 1995
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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C-THRU CORONARY GUIDE WIRE

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