K-number	K140849
Device name	ISOSEED
Applicant	Eckert & Ziegler Bebig GmbH
Product code	KXK
Device class	Class II
Decision date	Jul 2, 2014
Decision	Substantially Equivalent
Regulation	892.5730

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Source

View the full FDA submission: accessdata.fda.gov

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ISOSEED

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