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

    FORCEPS, HAEM, DEEP OPERATION, 20&22 CM.

    K Number: K770539 · Decision Apr 15, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    444
    Registration Numbers
    445
    Same Product Code
    103
    Applicant Total
    7
    Review Days
    25

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    Basic Information

    Device Name
    FORCEPS, HAEM, DEEP OPERATION, 20&22 CM.
    K Number
    K770539
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Sea-Pac Trading Corp.
    Date Received
    March 21, 1977
    Decision Date
    April 15, 1977
    Product Code
    GEN
    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
    GEN Forceps, General & Plastic Surgery

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    Other Clearances by Sea-Pac Trading Corp.

    K Number Device Name
    K770538 FORCEPS, HAEMOSTATIC, 14 16,&18 CM. LONG
    K770541 SCISSORS, SURGICAL, 12.5,14,16 & 18 CM.
    K770543 SCISSORS, SURGICAL, ANGULAR, 14 CM.
    K770542 SCISSORS, MAYO _TYLE, 14,16,18,20,22 CM.
    K770540 FORCEPS, MOSQUITO STYLE, 12.5 CM.
    K770544 SCISSORS, BANDAGE, 15,18,20CM., ANGULAR