Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K982944
    Date Cleared
    1998-11-19

    (90 days)

    Product Code
    Regulation Number
    878.4300
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    HEM-O-LOCK, MODEL 523935

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Hem-O-Lok® ligating clips are intended for use in procedures involving ligation of vessels or tissue structures. Surgeons should match clip size to the size of the vessel or tissue structure to be ligated.

    Device Description

    Weck Closure System's Hem-O-Lok® ligation clip is a manually applied hemostatic clip intended to connect internal tissues to aid healing. Hem-O-Lok® causes hemostasis through vessel ligation. The clip is nonabsorbable and is manufactured from polyacetal. The clips are housed in a cartridge and packaged in a rigid plastic blister with Tyvek coated lidding which is sold sterile. The method of sterilization will be EtO with a SAL of 10 . The blister packs are fitted into an overpack carton which serves as the sales unit.

    AI/ML Overview

    This document is a 510(k) Premarket Notification for the Hem-O-Lok® Ligation Clips. It states that the device is substantially equivalent to a previously cleared device (K941972) and details its intended use and technological characteristics. However, it does not contain any information regarding acceptance criteria or a study proving the device meets acceptance criteria.

    Therefore, I cannot provide the requested information from the provided text. The document is primarily a notification to the FDA for market clearance, focusing on substantial equivalence to a predicate device rather than detailing specific performance studies with acceptance criteria.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1