Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K990066
    Manufacturer
    Date Cleared
    1999-03-17

    (68 days)

    Product Code
    Regulation Number
    892.2030
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    CCD CAMERA, MODEL 9000

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

    This device is a Charge Coupled Device (CCD) video camera for use in digital radiography, including DSA, high resolution cardiology, and low dose fluoroscopy. It is designed for use with X-ray image intensifiers in diagnostic imaging chains.

    Device Description

    This device is a Charge Coupled Device (CCD) video camera for use in digital radiography, including DSA, high resolution cardiology, and low dose fluoroscopy. It is designed for use with X-ray image intensifiers in diagnostic imaging chains.

    AI/ML Overview

    The provided document is a 510(k) summary for the Camtronics CCD Camera, K990066. It claims substantial equivalence to a predicate device, K953974 MediCal Imaging Ltd. "Camvision 1000".

    However, the 510(k) summary explicitly states two crucial points:

    • "Performance data: Not required for determination of substantial equivalence for this class of device."
    • "Conclusions drawn from clinical and nonclinical test data: Not required for determination of substantial equivalence for this class of device."

    Therefore, based on the provided text, there is no acceptance criteria or study data presented that proves the device meets specific acceptance criteria in terms of performance metrics. The submission relies solely on demonstrating substantial equivalence to a predicate device through a comparison of specifications.

    Given this, I cannot provide the requested information in the format requested. The document does not contain:

    1. A table of acceptance criteria and the reported device performance: No performance data or acceptance criteria are reported.
    2. Sample sized used for the test set and the data provenance: No test set or data provenance is mentioned as performance data was not required.
    3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts: Not applicable, as no test set requiring ground truth was presented.
    4. Adjudication method: Not applicable.
    5. MRMC comparative effectiveness study: Not applicable.
    6. Standalone performance study: Not applicable.
    7. Type of ground truth used: Not applicable.
    8. Sample size for the training set: Not applicable, as this is a device submission, not an AI/ML algorithm submission in the modern sense.
    9. How the ground truth for the training set was established: Not applicable.

    Instead, the submission focuses on a direct comparison of technical specifications between the proposed device and the predicate device, as shown in the table below:

    Predicate Device Specifications Comparison (as presented in the 510(k) Summary)

    Principal Device (Camtronics CCD Camera)Predicate Device (K953974 MediVision-Medical Imaging Ltd. “Camvision 1000”)
    CCD and analog circuitry
    CCD typeinterlineinterline
    Scanningprogressiveprogressive
    Resolution1024 x 10241024 x 1024
    Contrast resolution12 bit, 4096 gray levels10 bit, 1024 gray levels
    Anti-bloomingautomatic control, up to 100:1automatic control, up to 100:1
    TV parameters
    Video outputHigh-line interlaced, 1.0 V peak to peak on 75 ohmcomposite video RS-343A or progressive scan, 50 or 60 Hz, 1.0 V peak-to-peak on 75 ohm
    Digital outputRS 644RS-422 AIA compatible
    Bandwidth12 bit 40 MHzinput equivalent to 20 MHz, output equivalent to 40 MHz
    Dynamic range66 dB60 dB
    Signal to noise ratiogreater than 1000:11000:1 at camera's connector
    Gammaadjustable or linearadjustable, 0.45-1.0
    Frame rateup to 25 or 30 frames per secondup to 25 or 30 frames per second
    Fast frame rate50 or 60 frames per second at 1024 x 512. 30 fps at 1024 x 102450 or 60 frames per second at 1024 x 512
    X-ray and image control
    Internal controlsautomatic gain control (AGC), automatic anti-blooming level (AAL)automatic gain control (AGC), automatic anti-blooming level (AAL), automatic integration control (AIC)
    External controlsvideo gain select, horizontal scan reverse, vertical scan reverse, black level selectvideo gain select, anti-blooming level select, horizontal scan reverse, vertical scan reverse, black level select
    Video synchronizationinternal or externalinternal or external
    Fluoroscopy controlautomatic brightness control (ABC)automatic brightness control (ABC)
    Iris controlmotorized controlautomatic control

    The conclusion of the 510(k) summary is that the Camtronics CCD Camera is "substantially equivalent to a legally marketed predicate device" and that "No new safety or effectiveness issues are raised." This determination is based on the "substantially equivalent technological characteristics, features, specifications, materials, modes of operation, and intended uses."

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1