K-number	K060752
Device name	ACMI DUR-HL LASER SYSTEMS
Applicant	Acmi Corporation
Product code	GEX
Device class	Class II
Decision date	May 25, 2006
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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ACMI DUR-HL LASER SYSTEMS

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