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

    BIPOLAR FORCEPS

    K Number: K023813 · Decision Jan 17, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    839
    Registration Numbers
    839
    Same Product Code
    2251
    Applicant Total
    142
    Review Days
    63

    Basic Information

    Device Name
    BIPOLAR FORCEPS
    K Number
    K023813
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4400
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    RICHARD WOLF MEDICAL INSTRUMENTS CORP.
    Date Received
    November 15, 2002
    Decision Date
    January 17, 2003
    Product Code
    GEI
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GEI Electrosurgical, Cutting & Coagulation & Accessories

    Similar 510(k) Clearances

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

    DENSITY; DENZA; DENSITY Noir

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    HybridAPC probe

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Electrosurgical Pads

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    EndyMed PRO MAX

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    DELPHI System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    gi2000 Electrosurgical Generator

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery
    View all

    Other Clearances by RICHARD WOLF MEDICAL INSTRUMENTS CORP.

    K Number Device Name
    K151282 core nova Complete Operating Room Endoscopy
    K130423 THE RICHARD WOLF ENDOCAM LOGIC HD CAMERA SYSTEM 5525
    K121724 ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2
    K120898 KEYPORT SYSTEM, INCLUDES: KEYPORT SILICONE SEALING INSERT 8850XXX KEYPORT TRUCAR 8850XX KEYPORT TROCAR 8850XX SEALING CA
    K090776 MEGAPULSE LASER SYSTEM AND FIBERS
    K080617 POWER DRIVE ART1 2304 WITH MOTOR HANDLES, TOOLS AND ACCESSORIES
    K080977 3 CCD ENDOCAM 5550
    K071292 VIEW MD OFFICE SYSTEM, MODEL 41066.5540
    K062720 S-LINE BIPOLAR RESECTOSCOPES AND BIPOLAR ELECTRODES
    K051276 HYSAFE MICRO MODULAR FORCEPS AND SCISSORS SYSTEM
    Search all 142 clearances from RICHARD WOLF MEDICAL INSTRUMENTS CORP. →