K-number	K083531
Device name	LIQUIBAND ULTIMA, MODEL LB0004
Applicant	Medlogic Global , Ltd.
Product code	MPN
Device class	Class II
Decision date	Feb 12, 2009
Decision	Substantially Equivalent
Regulation	878.4010

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View the full FDA submission: accessdata.fda.gov

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LIQUIBAND ULTIMA, MODEL LB0004

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