K-number	K922388
Device name	WATERS(TM) LC MODULE I FOR CLINICAL USE
Applicant	Millipore Corp.
Product code	LDM
Device class	Class I
Decision date	Sep 11, 1992
Decision	Substantially Equivalent
Regulation	862.2260

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View the full FDA submission: accessdata.fda.gov

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WATERS(TM) LC MODULE I FOR CLINICAL USE

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