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

    V. MUELLER (R) GOOSENECK CIRCULAR STAPLER

    K Number: K862772 · Decision Aug 18, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    76
    Registration Numbers
    76
    Same Product Code
    41
    Applicant Total
    31
    Review Days
    27

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    Basic Information

    Device Name
    V. MUELLER (R) GOOSENECK CIRCULAR STAPLER
    K Number
    K862772
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4740
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    American V. Mueller
    Date Received
    July 22, 1986
    Decision Date
    August 18, 1986
    Product Code
    GAG
    Advisory Committee
    General Hospital
    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
    GAG Stapler, Surgical

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    Other Clearances by American V. Mueller

    K Number Device Name
    K873771 HEYER-SCHULTE(R) ONE PIECE SHUNT VENT. CATH. INTRO
    K873332 MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM
    K871685 HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYS
    K864676 HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM
    K861471 V. MUELLER VITAL CLIP-HEMOSTATIC CLIP
    K854568 V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP
    K854049 HEYER-SCHULTE SYRINGO PERITONEAL SHUNT
    K851082 V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES
    K851974 V. MUELLER VITAL SKIN STAPLER
    K850947 V-MUELLER INVERTED LINEAR ANASTOMOSIS INSTRUMENTS
    Search all 31 clearances from American V. Mueller →