K-number	K022059
Device name	MICROVASIVE PULMONARY GUIDEWIRE
Applicant	Boston Scientific Corp
Product code	MDM
Device class	Class I
Decision date	Nov 13, 2002
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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MICROVASIVE PULMONARY GUIDEWIRE

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