K-number	K170183
Device name	Cetus system, Cetus probe
Applicant	A.R.C Laser GmbH
Product code	HQE
Device class	Class II
Decision date	Sep 27, 2017
Decision	Substantially Equivalent
Regulation	886.4150

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View the full FDA submission: accessdata.fda.gov

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Cetus system, Cetus probe

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