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

    VASCULAR CLAMP

    K Number: K881158 · Decision Jun 20, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    186
    Registration Numbers
    186
    Same Product Code
    203
    Applicant Total
    27
    Review Days
    94

    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
    VASCULAR CLAMP
    K Number
    K881158
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4450
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    T. Korossurgical Instruments Corp.
    Date Received
    March 18, 1988
    Decision Date
    June 20, 1988
    Product Code
    DXC
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DXC Clamp, Vascular

    Similar 510(k) Clearances

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

    Fogarty Spring Clips, Handleless Clamps, and Clamp Inserts

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Arc Adjustable Radial Cuff Compression Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Life Saving Tourniquet

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Namic Radial Arm Band, 23 cm (DYNJRADBAND); Namic Radial Arm Band, 26 cm (DYNJRADBANDL)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Radial Compression Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular
    View all

    Other Clearances by T. Korossurgical Instruments Corp.

    K Number Device Name
    K001915 GRAFT MARKER RING
    K002755 NON-ABSORBING STERNATOMY MONOFILAMENT SUTURE
    K954016 VIDEOSCOPE W/IRRIGATION SHEATH
    K953998 DISCETOME TISSUE ASPIRATOR
    K954052 ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTES
    K954014 PERCUTANEOUS DISCECTOMY CANNULA SYSTEM
    K935529 CERVICAL SELF-RETAINING RETRACTOR
    K926585 THOROCOSCOPY SELF-RETAINING RETRACTOR
    K931262 REUSABLE/INTERCHANGEABLE SHAFT, ENDOSCOPIC SCISSOR
    K926583 REUSABLE ENDOSCOPIC SCISSORS, GRASPER-MONOPOLAR
    Search all 27 clearances from T. Korossurgical Instruments Corp. →