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510(k) Data Aggregation

    K Number
    K030414
    Date Cleared
    2003-04-09

    (61 days)

    Product Code
    Regulation Number
    872.3660
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Sultan Genie Ultra Hydrophilic Impression Material is intended for use as a dental impression material. The material is dispensed from an automatic mixing cartridge system and placed into dental impression trays (metal or plastic) and is used to accurately reproduce intra-oral structures (teeth & gums) to provide models for study and/or fabrication of prosthetic devices.

    Device Description

    Not Found

    AI/ML Overview

    This is a 510(k) clearance letter from the FDA for Sultan Genie™ Ultra Hydrophilic Impression Material, classifying it as substantially equivalent to a predicate device. This document does not contain information about acceptance criteria or a study proving the device meets acceptance criteria in the manner typically expected for an AI/ML medical device.

    The provided text pertains to a traditional dental impression material, not an AI/ML-based device. Therefore, the details requested (such as sample size for test/training sets, expert qualifications, HRMC studies, standalone performance, etc.) are not applicable to this submission.

    The "acceptance criteria" and "study" mentioned in the context of this document would refer to the standards for dental impression materials (e.g., rheology, dimensional stability, tear strength, hydrophilic properties, biocompatibility) and the non-clinical bench testing or potentially limited clinical evaluations demonstrating that the Sultan Genie™ material performs comparably to the identified predicate devices for its intended use.

    Based on the provided text, I cannot furnish the requested information because it is not an AI/ML device submission.

    However, I can extract the relevant information from this document:

    • Device Name: Sultan Genie™ Ultra Hydrophilic Impression Material
    • Intended Use: As a dental impression material, dispensed from an automatic mixing cartridge system, placed into dental impression trays (metal or plastic) to accurately reproduce intra-oral structures (teeth & gums) to provide models for study and/or fabrication of prosthetic devices.
    • 510(k) Number: K030414
    • Regulatory Class: II
    • Product Codes: ELW

    To reiterate, the questions posed in your prompt (e.g., sample size for test set, expert qualifications, MRMC study, standalone performance) are designed for AI/ML device submissions, which this document is not.

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