K-number	K030889
Device name	ULTRAEKOGEL MODELS EK 2000 & EK 2001
Applicant	Inmed Ltda.
Product code	MUI
Device class	Class II
Decision date	May 23, 2003
Decision	Substantially Equivalent
Regulation	892.1570

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View the full FDA submission: accessdata.fda.gov

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ULTRAEKOGEL MODELS EK 2000 & EK 2001

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