K-number	K832058
Device name	ANGIO-FLO CONTIN-ARTERIAL FLUSH DEV.
Applicant	Parke-Davis Co.
Product code	KRA
Device class	Class II
Decision date	Sep 12, 1983
Decision	Substantially Equivalent
Regulation	870.1210

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View the full FDA submission: accessdata.fda.gov

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ANGIO-FLO CONTIN-ARTERIAL FLUSH DEV.

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