K-number	K972951
Device name	HIPALLAUR 51
Applicant	Aurex Precious Metal Industries (Pty)Ltd
Product code	EJT
Device class	Class II
Decision date	Sep 5, 1997
Decision	Substantially Equivalent
Regulation	872.3060

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View the full FDA submission: accessdata.fda.gov

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HIPALLAUR 51

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