K-number	K142668
Device name	Lesion-Loc Iodine I-125 Seed/Needle
Applicant	Intramedical Imaging, LLC
Product code	KXK
Device class	Class II
Decision date	Nov 21, 2014
Decision	Substantially Equivalent
Regulation	892.5730

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Source

View the full FDA submission: accessdata.fda.gov

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Lesion-Loc Iodine I-125 Seed/Needle

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