BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

    BODYFLEX MASSAGER

    K Number: K952041 · Decision Aug 14, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    759
    Registration Numbers
    759
    Same Product Code
    99
    Applicant Total
    1
    Review Days
    105

    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
    BODYFLEX MASSAGER
    K Number
    K952041
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.5660
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Truro'S Ent.
    Date Received
    May 1, 1995
    Decision Date
    August 14, 1995
    Product Code
    ISA
    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
    ISA Massager, Therapeutic, Electric

    Similar 510(k) Clearances

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

    VMAT PRO

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    ShockPhysio Mobile (model SW3200 Basic)

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    BTL-094

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Omnispec ED1000

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    OW100S (model OW100S-US)

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    DolorClast Radial

    FDA 510(k)
    FDA Class 1 ·Physical Medicine
    View all