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

    UNIVERSAL BY RUSH-HAMPTON ARTHROSCOPIC

    K Number: K843282 · Decision Oct 22, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    7
    Registration Numbers
    7
    Same Product Code
    5
    Applicant Total
    1
    Review Days
    63

    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
    UNIVERSAL BY RUSH-HAMPTON ARTHROSCOPIC
    K Number
    K843282
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    874.4680
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Applicant
    Rush Hampton Industries
    Date Received
    August 20, 1984
    Decision Date
    October 22, 1984
    Product Code
    BWH
    Advisory Committee
    Ear, Nose, Throat
    Review Advisory Committee
    EN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    BWH Forceps, Biopsy, Bronchoscope (Non-Rigid)

    Similar 510(k) Clearances

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

    Radial Jaw 4 Pulmonary Biopsy Forceps

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    RADIAL JAW 4 PULMONARY BIOPSY FORCEPS

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    RADIAL JAW 4 PULMONARY STANDARD CAPACITY BIOPSY FORCEPS; RADIAL JAW 4 PULMONARY STANDARD CAPACITY BIOPSY FORCEPS WITH NE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    REUSABLE BRONCHIAL BIOPSY FORCEPS

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    WILTEK BIOPSY FORCEPS

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat
    View all