K-number	K811171
Device name	VASCULON II I.V. CATHETER
Applicant	Pioneer Viggo, Inc.
Product code	FOZ
Device class	Class II
Decision date	May 27, 1981
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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VASCULON II I.V. CATHETER

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