K-number	K833716
Device name	LP200 & HP800 SERIES VASCULAR PROSTH
Applicant	Intervascular, Inc.
Product code	DSY
Device class	Class II
Decision date	Jan 10, 1984
Decision	Substantially Equivalent
Regulation	870.3450

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View the full FDA submission: accessdata.fda.gov

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LP200 & HP800 SERIES VASCULAR PROSTH

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