K-number	K990823
Device name	PVS 1400 GUIDEWIRE
Applicant	Precision Vascular Systems, Inc.
Product code	DQX
Device class	Class II
Decision date	Jul 23, 1999
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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PVS 1400 GUIDEWIRE

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