K-number	K093409
Device name	POWERPUMP ARTHROSCOPY SYSTEM
Applicant	Medical Vision AB
Product code	HRX
Device class	Class II
Decision date	Feb 24, 2010
Decision	Substantially Equivalent
Regulation	888.1100

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Source

View the full FDA submission: accessdata.fda.gov

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POWERPUMP ARTHROSCOPY SYSTEM

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