BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    AMBULATOR

    K Number: K921752 · Decision May 4, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    189
    Registration Numbers
    189
    Same Product Code
    34
    Applicant Total
    2
    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
    AMBULATOR
    K Number
    K921752
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.3100
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    The Anthros Medical Group
    Date Received
    April 13, 1992
    Decision Date
    May 4, 1992
    Product Code
    INM
    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
    INM Chair, With Casters

    Similar 510(k) Clearances

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

    NISSIN PEDIATRIC SERIES WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    STRYKER 5050 STRECHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    CAREMOR CLINER

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    RECLINING GERI CHAIRS W/CASTERS & LAP TRAY

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    BENCHES

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    CHAIRS

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

    Other Clearances by The Anthros Medical Group

    K Number Device Name
    K933060 S-610 & 2-628 WHEELED SHOWER STRETCHERS