K-number	K133757
Device name	GFS II STANDARD, GFS II LARGE, GFS MIMI
Applicant	Parcus Medical, LLC
Product code	MBI
Device class	Class II
Decision date	Feb 4, 2014
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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GFS II STANDARD, GFS II LARGE, GFS MIMI

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