K-number	K092471
Device name	MODEL SENTINELLA 102
Applicant	General Equipment For Medical Imaging, S.A.
Product code	IYX
Device class	Class I
Decision date	Oct 2, 2009
Decision	Substantially Equivalent
Regulation	892.1100

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View the full FDA submission: accessdata.fda.gov

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MODEL SENTINELLA 102

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