K-number	K053169
Device name	RM3 RENAL PRESERVATION SYSTEM
Applicant	Waters Instruments, Inc.
Product code	KDK
Device class	Class II
Decision date	Jan 17, 2006
Decision	Substantially Equivalent
Regulation	876.5880

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View the full FDA submission: accessdata.fda.gov

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RM3 RENAL PRESERVATION SYSTEM

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