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

    PERSONAL TRANSFER SYSTEM

    K Number: K885270 · Decision Mar 14, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    58
    Registration Numbers
    58
    Same Product Code
    20
    Applicant Total
    1
    Review Days
    82

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    PERSONAL TRANSFER SYSTEM
    K Number
    K885270
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5500
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Columbus Mckinnon Corp.
    Date Received
    December 22, 1988
    Decision Date
    March 14, 1989
    Product Code
    FNG
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FNG Lift, Patient, Ac-Powered

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (FNG), ordered by most recent decision date.

    HT-WEDGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HOVERJACK AIR PATIENT LIFT DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PATIENT SUPPORT SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    A.C. POWER PATIENT LIFT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SAF-LIFT/SAF-KARY

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PATIENT LIFT AND TRANSPORT

    FDA 510(k)
    FDA Class 2 ·General Hospital
    View all