K-number	K932301
Device name	FENWAL(R) 40/150 MICRON DUAL SCREEN FILTER
Applicant	Baxter Healthcare Corp
Product code	FPB
Device class	Class II
Decision date	Nov 10, 1993
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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FENWAL(R) 40/150 MICRON DUAL SCREEN FILTER

Everything you need for a 510(k) submission. Nothing you don't.