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SINUS DILATION SYSTEM WITH CANNULATED INSTRUMENT

Arthrocare Corp. · Class I · Cleared Oct 4, 2013

K-numberK131709
Device nameSINUS DILATION SYSTEM WITH CANNULATED INSTRUMENT
ApplicantArthrocare Corp.
Product codeLRC
Device classClass I
Decision dateOct 4, 2013
DecisionSubstantially Equivalent
Regulation874.4420
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View the full FDA submission: accessdata.fda.gov

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