K-number	K012660
Device name	GIMMI'ALPHA' ENDOSCOPES & ACCESSORIES
Applicant	Gimmi GmbH
Product code	FET
Device class	Class II
Decision date	Dec 20, 2001
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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GIMMI'ALPHA' ENDOSCOPES & ACCESSORIES

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