BEUDAMED
    FDA 510(k) Unknown 🇺🇸 United States

    CUSTOM PROCEDURE KIT (VARIOUS SUB-TITLES)

    K Number: K861198 · Decision May 16, 1986
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    7
    Review Days
    46

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    Basic Information

    Device Name
    CUSTOM PROCEDURE KIT (VARIOUS SUB-TITLES)
    K Number
    K861198
    Clearance Type
    Traditional
    Decision
    Unknown
    Applicant
    Quali-Med, Inc.
    Date Received
    March 31, 1986
    Decision Date
    May 16, 1986
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N

    Other Clearances by Quali-Med, Inc.

    K Number Device Name
    K871408 BLOOD VESSEL CONNECTOR
    K862972 DISPOSABLE MIRROR
    K862472 QUARTZ RODS TITANIUM RODS
    K862241 STANDARD BASIN KIT CUSTOM BASIN KIT
    K862242 PAP SMEAR KIT
    K862172 QUALI-MED'S OPERATING ROOM DRAPES