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510(k) Data Aggregation

    K Number
    K101768
    Manufacturer
    Date Cleared
    2010-10-05

    (104 days)

    Product Code
    Regulation Number
    892.1200
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The ECAM SCINTRON Gamma Camera System for diagnostic nuclear medicine is used to perform static, dynamic and gated studies (non positron emitting tomography), as well as SPECT or planar procedure on standing, seated or recumbent patients.

    Device Description

    The ECAM SCINTRON Gamma Camera System is a remanufactured Siemens Gamma Camera with MiE Workstation. It is designed for diagnostic nuclear medicine used to perform static, dynamic and gated studies (non positron emitting tomography), as well as SPECT or planar procedure on standing, seated or recumbent patients.

    The ECAM SCINTRON Gamma Camera System is substantially equivalent to the legally market device e.cam, K963983, from Siemens and our device SCINTRON, K101013.

    The changes incorporated into the remanufactured ECAM Gamma Camera include economical and ecological issues. This closes the gap between more durable electronics and mechanics lifetimes and shortened development cycles.

    AI/ML Overview

    This document is a 510(k) summary for the ECAM SCINTRON Gamma Camera System. It states that the device is substantially equivalent to a predicate device but does not include any acceptance criteria, performance data, or details of a study that proves the device meets specific acceptance criteria as requested in your input.

    Therefore, I cannot provide the requested information from the provided text. The document focuses on regulatory approval based on substantial equivalence to existing devices rather than new performance studies with specific criteria.

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