K-number	K011581
Device name	AMERITEK BRACHYTHERAPY TEMPLATE
Applicant	Amertek Medical, Inc.
Product code	ITX
Device class	Class II
Decision date	Jul 17, 2001
Decision	Substantially Equivalent
Regulation	892.1570

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View the full FDA submission: accessdata.fda.gov

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AMERITEK BRACHYTHERAPY TEMPLATE

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