K-number	K003512
Device name	LASER PACK I, LASER PACK II, PHACO PACK I, PHACO PACK II
Applicant	A.R.C. Laser AG
Product code	HQC
Device class	Class II
Decision date	Feb 8, 2001
Decision	Substantially Equivalent
Regulation	886.4670

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View the full FDA submission: accessdata.fda.gov

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LASER PACK I, LASER PACK II, PHACO PACK I, PHACO PACK II

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