K-number	K072404
Device name	ERBE ERBEJET 2 SYSTEM
Applicant	Erbe USA, Inc.
Product code	FQH
Device class	Class II
Decision date	Oct 31, 2007
Decision	Substantially Equivalent
Regulation	880.5475

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View the full FDA submission: accessdata.fda.gov

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ERBE ERBEJET 2 SYSTEM

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