K-number	K110426
Device name	DYNA-EXTOR II
Applicant	Bk Meditech, Co., Ltd.
Product code	KTT
Device class	Class II
Decision date	Nov 2, 2011
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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DYNA-EXTOR II

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