K-number	K033781
Device name	BEBIG ISOSEED I-125
Applicant	Bebig Isotopen-Und Medizintechnik GmbH
Product code	KXK
Device class	Class II
Decision date	Dec 30, 2003
Decision	Substantially Equivalent
Regulation	892.5730

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View the full FDA submission: accessdata.fda.gov

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BEBIG ISOSEED I-125

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