K-number	K053616
Device name	POLARIS WR, ST APPLICATOR
Applicant	Syneron Medical, Ltd.
Product code	GEX
Device class	Class II
Decision date	Mar 14, 2006
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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POLARIS WR, ST APPLICATOR

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