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510(k) Data Aggregation

    K Number
    K981441
    Date Cleared
    1998-07-10

    (80 days)

    Product Code
    Regulation Number
    870.1200
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    HEART CATH TRAY, STERILE, DISPOSABLE

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

    Trinity's Heart Cath Tray is a sterile prepackaged disposable unit. It contains the non-reinforced gowns, femoral angio drape, OR cloth towels, absorbent towels, 16 oz sponge bowl, 32 oz sponge bowls, bowl guidewire with lid, 2 oz medicine cups, gauze sponges, straight mosquito forceps, 25 ga x 5/8" needle, 22 ga x 1 1/2" needle, 5cc L/L syringe, 10cc L/L syringe, 20cc L/L syringe, 10cc L/S syringes, towel clips, #11 blade scalpel, table cover, and band bag, neccessary for the performance of the Heart Cath surgical procedure..

    Device Description

    Trinity's Heart Cath Tray is a sterile prepackaged disposable unit. It contains the non-reinforced gowns, femoral angio drape, OR cloth towels, absorbent towels, 16 oz sponge bowl, 32 oz sponge bowls, bowl guidewire with lid, 2 oz medicine cups, gauze sponges, straight mosquito forceps, 25 ga x 5/8" needle, 22 ga x 1 1/2" needle, 5cc L/L syringe, 10cc L/L syringe, 20cc L/L syringe, 10cc L/S syringes, towel clips, #11 blade scalpel, table cover, and band bag, neccessary for the performance of the Heart Cath surgical procedure..

    AI/ML Overview

    This document is a 510(k) clearance letter from the FDA for a medical device called "Heart Cath Tray". It is not a study report or a technical document describing acceptance criteria and device performance. Therefore, I cannot extract the requested information.

    The document states that the device is "substantially equivalent" to legally marketed predicate devices, which means its safety and effectiveness are considered to be similar to devices already on the market. However, it does not provide details of specific performance criteria or the results of a study to demonstrate those criteria.

    To answer your questions, I would need a technical report, a clinical study summary, or a comprehensive PMA/510(k) submission that details the performance data and acceptance criteria for the device.

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