K-number	K122302
Device name	ACE MAGNESIUM REGENT
Applicant	Alfa Wassermann Diagnostics Technologies, LLC
Product code	JGJ
Device class	Class I
Decision date	Aug 27, 2012
Decision	Substantially Equivalent
Regulation	862.1495

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Source

View the full FDA submission: accessdata.fda.gov

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ACE MAGNESIUM REGENT

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