K-number	K982271
Device name	WAKO DIRECT LDL-C
Applicant	Wako Chemicals USA, Inc.
Product code	MRR
Device class	Class I
Decision date	Sep 22, 1998
Decision	Substantially Equivalent
Regulation	862.1475

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View the full FDA submission: accessdata.fda.gov

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WAKO DIRECT LDL-C

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