K-number	K012826
Device name	BIOPORTA G, MODEL 2052
Applicant	Wieland Edelmetalle GmbH & Co.
Product code	EJT
Device class	Class II
Decision date	Nov 1, 2001
Decision	Substantially Equivalent
Regulation	872.3060

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View the full FDA submission: accessdata.fda.gov

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BIOPORTA G, MODEL 2052

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