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

    CAMINO HAND DRILL - MODEL 030

    K Number: K862160 · Decision Jul 18, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    57
    Registration Numbers
    57
    Same Product Code
    16
    Applicant Total
    18
    Review Days
    42

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    Basic Information

    Device Name
    CAMINO HAND DRILL - MODEL 030
    K Number
    K862160
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.4300
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Applicant
    Camino Laboratories, Inc.
    Date Received
    June 6, 1986
    Decision Date
    July 18, 1986
    Product Code
    HBG
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HBG Drills, Burrs, Trephines & Accessories (Manual)

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    Other Clearances by Camino Laboratories, Inc.

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    K920088 CAMINO VENTRICULAR NEEDLE
    K914735 VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM
    K912833 CAMINO MODEL M420: MONIT INTER W/MEAN PRES DISPLAY
    K893232 MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM
    K881183 VENTRICULAR BOLT PRESSURE MONITORING KIT #110-4H
    K863969 CAMINO COMPARTMENTAL PRESS MONITOR CATH/110-4D
    K861961 CAMINO CSF DRAINAGE SYSTEM MODEL 040
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