K-number	K935997
Device name	PLATINUM PLUS GUIDEWIRE
Applicant	Boston Scientific Corp
Product code	DQX
Device class	Class II
Decision date	Jun 17, 1994
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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PLATINUM PLUS GUIDEWIRE

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