K-number	K792174
Device name	MODEL DM 353 & DM-353-L SINGLE NEEDLE
Applicant	Extracorporeal Medical Specialities, Inc.
Product code	FIF
Device class	Class II
Decision date	Nov 16, 1979
Decision	Substantially Equivalent
Regulation	876.5820

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View the full FDA submission: accessdata.fda.gov

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MODEL DM 353 & DM-353-L SINGLE NEEDLE

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