BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    SPORIDIDIN-D COLD STERILIZING/SOLUTION

    K Number: K830722 · Decision Jun 30, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    7
    Registration Numbers
    7
    Same Product Code
    56
    Applicant Total
    8
    Review Days
    114

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    Basic Information

    Device Name
    SPORIDIDIN-D COLD STERILIZING/SOLUTION
    K Number
    K830722
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5820
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Sporicidin Intl.
    Date Received
    March 8, 1983
    Decision Date
    June 30, 1983
    Product Code
    LIF
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LIF Dialyzer Reprocessing System

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    Other Clearances by Sporicidin Intl.

    K Number Device Name
    K003087 MODIFICATION TO SPORICIDIN STERILIZING AND DISINFECTING SOLUTION
    K983194 SPORICIDIN STERILIZING AND DISINFECTING SOLUTION (SSDS)
    K926013 SPORICIDIN BRAND DISINFECT TOWEL, SPRAY/SOLUT MODI
    K922262 SPORICIDIN BRAND DISINFECT TOWELETTES/SPRAY/SOLUT
    K904581 SPORICIDIN BRAND DISINFECTANT SOLUTION
    K904580 SPORICIDIN BRAND DISINFECTANT SPRAY
    K904579 SPORICIDIN BRAND DISINFECTANT TOWELETTES