K-number	K112548
Device name	ALTOMEC ARTHROSCOPE
Applicant	Altomec Endoscopy, Inc.
Product code	HRX
Device class	Class II
Decision date	Aug 15, 2012
Decision	Substantially Equivalent
Regulation	888.1100

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Source

View the full FDA submission: accessdata.fda.gov

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ALTOMEC ARTHROSCOPE

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