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

    MASSAGE TABLE AAT-100

    K Number: K832464 · Decision Aug 16, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    6
    Registration Numbers
    6
    Same Product Code
    65
    Applicant Total
    79
    Review Days
    21

    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
    MASSAGE TABLE AAT-100
    K Number
    K832464
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.5880
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    R&D Systems, Inc.
    Date Received
    July 26, 1983
    Decision Date
    August 16, 1983
    Product Code
    JFB
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JFB Table, Physical Therapy, Multi Function

    Similar 510(k) Clearances

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

    Ceragem Automatic Thermal Massager (CGM MB-2401)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    AGILIS - Multi-function Physical Therapy Table (Model: Plus, Pro and Basic.)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Ceragem Automatic Thermal Massager (CGM MB-2301 & CGM MB-2302)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Ceragem Automatic Thermal Massager (CGM-MB-1902)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    N7-S

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Ceragem Automatic Thermal Massager, Model CGM MB-1701 & CGM MB-1702

    FDA 510(k)
    FDA Class 2 ·Physical Medicine
    View all

    Other Clearances by R&D Systems, Inc.

    K Number Device Name
    K160606 BC-5D Hematology Control
    K130962 R&D 5D RETIC HEMATOLOGY CONTROL
    K101578 R&D SYSTEMS BODY FLUID-I HEMATOLOGY CONTROL
    K100050 R & D SYSTEMS XERET HEMATOLOGY CONTROL
    K091433 R&D SYSTEMS TETIC-I PLUS HEMOTOLOGY CONTROL
    K073178 HCT EXTENDED HEMATOLOGY CONTROL, MODEL HCT004
    K072846 CSF AUTOMATED CONTROL, MODELS CSF001, CSF003
    K072268 HC WBC HEMATOLOGY CONTROL, MODEL: WBC00S
    K072096 CBC-5D PLUS RETICS HEMATOLOGY CONTROL, MODELS: 5DR03, 5DR04
    K070334 R&D SICKLE QC CONTROL
    Search all 79 clearances from R&D Systems, Inc. →