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REDSENSE-HOME USE

Redsense Medical AB · Class II · Cleared May 10, 2010

K-numberK092955
Device nameREDSENSE-HOME USE
ApplicantRedsense Medical AB
Product codeODX
Device classClass II
Decision dateMay 10, 2010
DecisionSubstantially Equivalent
Regulation876.5820
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Source

View the full FDA submission: accessdata.fda.gov

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