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K/K (ASMA/ANA) UNIVERSAL BIOPAK

Bioware Products · Class II · Cleared Jan 29, 1981

K-numberK802299
Device nameK/K (ASMA/ANA) UNIVERSAL BIOPAK
ApplicantBioware Products
Product codeDHN
Device classClass II
Decision dateJan 29, 1981
DecisionSubstantially Equivalent
Regulation866.5100
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View the full FDA submission: accessdata.fda.gov

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