K-number	K233090
Device name	DEKA AGAIN PRO family
Applicant	El.En S.P.A.
Product code	GEX
Device class	Class II
Decision date	Oct 27, 2023
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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DEKA AGAIN PRO family

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