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

    JACOBS HIGH VACUUM SUCTION UNIT 05-2570

    K Number: K843693 · Decision Oct 31, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    98
    Registration Numbers
    98
    Same Product Code
    158
    Applicant Total
    18
    Review Days
    42

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    Basic Information

    Device Name
    JACOBS HIGH VACUUM SUCTION UNIT 05-2570
    K Number
    K843693
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4780
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    J. Sklar Mfg. Co., Inc.
    Date Received
    September 19, 1984
    Decision Date
    October 31, 1984
    Product Code
    BTA
    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
    BTA Pump, Portable, Aspiration (Manual Or Powered)

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    Other Clearances by J. Sklar Mfg. Co., Inc.

    K Number Device Name
    K842112 TISCHLER CERVICAL BIOPSY PUNCH FORCEPS
    K842111 KOGAN ENDOSPECULUM 9-1/2
    K822448 SCISSORS, VARIOUS
    K802457 KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610
    K802458 KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611
    K801273 MAGILL CATHETER INTRO. FORCEPS
    K800441 RUDD-CLINIC HEMORRHOIDAL FORCEPS
    K790577 HEMORRHOIDAL LIGATOR
    K772230 CANNULA, PERFUSION, FALLOPIAN TUBE
    K772229 MINICLAMPS, STABILIZ., FALLOPIAN TUBE
    Search all 18 clearances from J. Sklar Mfg. Co., Inc. →