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

    LP-5

    K Number: K844179 · Decision Jan 18, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    130
    Registration Numbers
    130
    Same Product Code
    504
    Applicant Total
    10
    Review Days
    84

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    Basic Information

    Device Name
    LP-5
    K Number
    K844179
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5895
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Life Products, Inc.
    Date Received
    October 26, 1984
    Decision Date
    January 18, 1985
    Product Code
    CBK
    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
    CBK Ventilator, Continuous, Facility Use

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    Other Clearances by Life Products, Inc.

    K Number Device Name
    K901714 LIFESTYLE HOME TANNING UNITS
    K854022 LPA-1 PRESSURE MONITOR
    K850151 L100B UNIVERSAL & L100A NIGHT PATIENT CIRCUIT
    K851905 LPA-2 REMOTE ALARM
    K851805 LPA-3 PRINTER
    K842122 4A
    K844081 LP4 VENTILATOR
    K844290 L100D PATIENT CIRCUIT DUAL LINE
    K770132 MODEL LP-3 PORTABLE VOLUME VENTILATOR