K-number	K173311
Device name	ARTHRO-Pump PA304
Applicant	W.O.M. World of Medicine GmbH
Product code	HRX
Device class	Class II
Decision date	May 9, 2018
Decision	Substantially Equivalent
Regulation	888.1100

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Source

View the full FDA submission: accessdata.fda.gov

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ARTHRO-Pump PA304

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