K-number	K012189
Device name	ANGELTOUCH VENTED IV ADMINISTRATION SET
Applicant	Angiplast Private , Ltd.
Product code	LHI
Device class	Class II
Decision date	Mar 5, 2002
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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ANGELTOUCH VENTED IV ADMINISTRATION SET

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