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

    HOLGRATH COMBINED SPINAL EPIDURAL NEEDLE SET

    K Number: K954835 · Decision Jan 31, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    81
    Registration Numbers
    81
    Same Product Code
    154
    Applicant Total
    6
    Review Days
    103

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    Basic Information

    Device Name
    HOLGRATH COMBINED SPINAL EPIDURAL NEEDLE SET
    K Number
    K954835
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5140
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Holgrath Medical Technologies, Inc.
    Date Received
    October 20, 1995
    Decision Date
    January 31, 1996
    Product Code
    CAZ
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    CAZ Anesthesia Conduction Kit

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    Other Clearances by Holgrath Medical Technologies, Inc.

    K Number Device Name
    K946047 HOLGRATH METAL-HUB, EPIDURAL NEEDLE
    K944906 HOLGRATH PLASTIC-HUB EPIDURAL NEEDLE
    K944905 HOLGRATH PLASTIC-HUB, WHITACRE STYLE SPINAL NEEDLE
    K944908 HOLGRATH PLASTIC-HUB, COICAL POINT SPINAL NEEDLE
    K944907 HOLGRATH PLASTIC-HUB, QUINCKE SPINAL NEEDLE