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510(k) Data Aggregation

    K Number
    K984013
    Manufacturer
    Date Cleared
    1999-01-26

    (76 days)

    Product Code
    Regulation Number
    872.6640
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    PLANMECA INTRACAM STATION

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

    The Planmeca Intracam Station intra oral video camera system is intended for use by practitioners in the dental field for use as an aid or adjunct to assist in viewing intra oral anatomies and capturing and storing images for later retrieval. The camera interfaces with video printers, TV/monitors, capture boards etc. The Intracam Station is an independent system, i.e. it can be used separate from a dental unit.

    Device Description

    Planmeca Intracam Station intra oral video camera system

    AI/ML Overview

    I am sorry, but the provided text from the FDA 510(k) clearance letter for the Planmeca Intracam Station does not contain the information requested regarding acceptance criteria and details of a study proving device performance.

    The letter is a standard FDA clearance document, which:

    • Confirms substantial equivalence to a predicate device.
    • States the indications for use.
    • Outlines general regulatory requirements.

    It does not include:

    • A table of acceptance criteria.
    • Reported device performance metrics (e.g., sensitivity, specificity, accuracy).
    • Details about a specific study (sample sizes, data provenance, ground truth establishment, expert qualifications, adjudication methods, MRMC studies, or standalone performance).
    • Information about training sets.

    Therefore, I cannot fulfill your request based on the provided input.

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