K-number	K905497
Device name	MASTER FLOW I.V. PUMPETTE
Applicant	The Master Medical Corp.
Product code	LDR
Device class	Class II
Decision date	Apr 16, 1991
Decision	Substantially Equivalent
Regulation	880.5725

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View the full FDA submission: accessdata.fda.gov

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MASTER FLOW I.V. PUMPETTE

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