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

    PROFESSIONAL SUPPLIES, INC.LENS CARRYING CASE

    K Number: K850046 · Decision Apr 15, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    73
    Applicant Total
    2
    Review Days
    98

    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
    PROFESSIONAL SUPPLIES, INC.LENS CARRYING CASE
    K Number
    K850046
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    Professional Supplies, Inc.
    Date Received
    January 7, 1985
    Decision Date
    April 15, 1985
    Product Code
    HPX
    Advisory Committee
    Unknown
    Review Advisory Committee
    OP
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HPX Lens, Contact (Polymethylmethacrylate)

    Similar 510(k) Clearances

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

    PMMA CLASIC

    FDA 510(k)
    FDA Unclassified ·Unknown

    KERATOPLASTY SUTURING LENS

    FDA 510(k)
    FDA Unclassified ·Unknown

    MULTI-VIEW BIFOCALS

    FDA 510(k)
    FDA Unclassified ·Unknown

    MARTIN-HENSLEY SEGMENT LENS

    FDA 510(k)
    FDA Unclassified ·Unknown

    OPTIKEM PMMA CONTACT LENS

    FDA 510(k)
    FDA Unclassified ·Unknown

    ILLUMINATING INFUSION CONTACT LENS FOR EYE SURGERY

    FDA 510(k)
    FDA Unclassified ·Unknown
    View all

    Other Clearances by Professional Supplies, Inc.

    K Number Device Name
    K832327 SILA CLEAN 20/20