K-number	K111488
Device name	MANTARAY GUIDEWIRE MODEL M-6000, M-6001, M-6002, M-6003
Applicant	Bridgepoint Medical
Product code	DQX
Device class	Class II
Decision date	Jun 30, 2011
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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MANTARAY GUIDEWIRE MODEL M-6000, M-6001, M-6002, M-6003

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