K-number	K801173
Device name	ANGIO-FLO MONITORING KIT
Applicant	Hospital Products Co.
Product code	KRA
Device class	Class II
Decision date	May 28, 1980
Decision	Substantially Equivalent
Regulation	870.1210

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View the full FDA submission: accessdata.fda.gov

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ANGIO-FLO MONITORING KIT

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