K-number	K060897
Device name	EMBEDDING TOOL, MODEL TE-1000
Applicant	Medigroup, Inc.
Product code	FJS
Device class	Class II
Decision date	Jul 18, 2006
Decision	Substantially Equivalent
Regulation	876.5630

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View the full FDA submission: accessdata.fda.gov

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EMBEDDING TOOL, MODEL TE-1000

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