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AURORA SR AND SRA APPLICATOR

Syneron Medical, Ltd. · Class II · Cleared Mar 9, 2005

K-numberK050452
Device nameAURORA SR AND SRA APPLICATOR
ApplicantSyneron Medical, Ltd.
Product codeGEX
Device classClass II
Decision dateMar 9, 2005
DecisionSubstantially Equivalent
Regulation878.4810
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View the full FDA submission: accessdata.fda.gov

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