K-number	K123441
Device name	STRYKER CROSSFLOW ARTHROSCOPY PUMP
Applicant	Stryker Endoscopy
Product code	HRX
Device class	Class II
Decision date	Jan 9, 2013
Decision	Substantially Equivalent
Regulation	888.1100

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Source

View the full FDA submission: accessdata.fda.gov

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STRYKER CROSSFLOW ARTHROSCOPY PUMP

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