K-number	K871180
Device name	ARTHRO AUTOMAT 5002
Applicant	F.M. Wiest USA, Inc.
Product code	HRX
Device class	Class II
Decision date	Sep 29, 1987
Decision	Substantially Equivalent
Regulation	888.1100

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View the full FDA submission: accessdata.fda.gov

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ARTHRO AUTOMAT 5002

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