K-number	K060404
Device name	AG-PLUS, MODEL 91210
Applicant	Medel S.P.A.
Product code	CAF
Device class	Class II
Decision date	Jun 22, 2006
Decision	Substantially Equivalent
Regulation	868.5630

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View the full FDA submission: accessdata.fda.gov

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AG-PLUS, MODEL 91210

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