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510(k) Data Aggregation

    K Number
    K051742
    Manufacturer
    Date Cleared
    2005-10-07

    (101 days)

    Product Code
    Regulation Number
    884.6100
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    OOCYTE RETRIEVAL NEEDLE SET, MODELS 917-IH AND 917-SH

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

    The InnTec, Inc. Oocyte Retrieval Needle Set is an assisted reproduction needle indicated for used and intended to be used for obtaining female gametes / oocytes from the body.

    Device Description

    The Oocyte Retrieval Needle Sets are sterile, single patient use, disposable devices supporting obtaining female gametes/oocytes from the body. The Oocyte Retrieval Needle Sets are packaged in a commercially available, sterile barrier pouch.

    AI/ML Overview

    This document describes a 510(k) premarket notification for Oocyte Retrieval Needle Sets. This type of submission focuses on demonstrating substantial equivalence to a legally marketed predicate device, rather than proving the device meets specific acceptance criteria through a clinical study.

    Therefore, the requested information regarding acceptance criteria, study details, sample sizes, ground truth, experts, and MRMC studies is not applicable to this type of regulatory submission.

    The document explicitly states:

    • "The technology of the device is the same as the predicate."
    • "Concesses of the manufacturing processes of the InnTec, Inc. Oocyte Retrieval Needle Sets are the same as the predicate device. No new questions of safety or effectiveness are raised."
    • "FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies."

    This indicates that the submission relies on the established safety and effectiveness of the predicate device, and no new studies were conducted to define or meet specific performance acceptance criteria for this particular device.

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