K-number	K984235
Device name	INTERSOURCE 125, MODEL 1251L
Applicant	International Brachytherapy, Inc.
Product code	KXK
Device class	Class II
Decision date	Jun 9, 1999
Decision	Substantially Equivalent
Regulation	892.5730

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View the full FDA submission: accessdata.fda.gov

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INTERSOURCE 125, MODEL 1251L

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