K-number	K111483
Device name	JOULE CLEARSENSE LASER SYSTEM
Applicant	Sciton, Inc
Product code	PDZ
Device class	Class II
Decision date	Dec 7, 2011
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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JOULE CLEARSENSE LASER SYSTEM

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