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510(k) Data Aggregation

    K Number
    K992280
    Manufacturer
    Date Cleared
    1999-09-03

    (58 days)

    Product Code
    Regulation Number
    892.1710
    Reference & Predicate Devices
    Predicate For
    N/A
    Why did this record match?
    Reference Devices :

    K934870,K973631

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

    The 1-650 Mammography System is intended to produce radiographic images of the breast. Its specific intended use is for screening and diagnostic mammography. Screening mammography involves the production of images for initial examination for breast cancer diagnosis. Diagnostic mammography includes the production of magnified images for more thorough examination of areas of the breast determined suspicious through screening mammography, special views, spot compression views, and the production of images used by a physician in preparation for biopsy.

    Device Description

    The Lorad I-650 mammography system is based on Lorad's currently marketed D-550 (K934870) and Elite (K973631) Dedicated Mammographic Systems. The mechanical packaging is similar to the D-550, while the electronics are similar to the Elite. The Lorad I-650 is a standalone mammography device, mounted on a base to be permanently mounted in position. The unit is AC powered, and must be connected to a 220 VAC/50-60 Hertz (nominal) line to operate. The standalone unit has two major assemblies: The C-arm and the Gantry. The C-arm, which contains the x-ray tube, an image receptor support, compression device, a beam limiting device, switches that actuate the C-arm functions, and sensors for detecting installed accessories and making radiation measurements, is attached to the front (patient side) of the Gantry. The C-arm frame is constructed of two vertical steel rails, which are precision machined to accept the components which it supports. Molded plastic covers enclose the x-ray tube, which is purchased from OEM manufacturers, and the beam limiting device, while aluminum covers enclose the sides, back, top and bottom of the C-arm framework. The C-arm is attached by a locking pivot mechanism to the Gantry. The pivot allows the C-arm to be manually rotated about its axis. The pivot mechanism is attached to the Gantry via a vertically moving carriage. This carriage is capable of movement in the vertical direction, driven by an AC motor and a drive screw mounted to the base of the Gantry. The pivoting action of the C-arm is locked by an electromagnetic brake attached to the vertical carriage, which, in its unactuated condition, prevents rotation. The brake must be electrically actuated to release the C-arm for movement. The Gantry is constructed of a welded steel frame, to which the electrical assemblies and components of the unit are mounted. The operator control is mounted on the side panel of the Gantry, or may be mounted remotely. The input power and input circuit breaker are located on the lower rear panel of the Gantry.

    AI/ML Overview

    This document describes the Lorad I-650 Mammography System. Here's an analysis of the provided text for acceptance criteria and the study proving it:

    Key Takeaway: This document is a 510(k) summary for a mammography system. The "acceptance criteria" are primarily regulatory and performance specifications for the device itself, rather than acceptance criteria for an AI algorithm. The "study" described is a series of bench tests to verify these specifications, not a clinical trial involving human readers or AI performance.


    Acceptance Criteria and Device Performance (Table)

    The document outlines numerous specifications for the Lorad I-650 Mammography System, which serve as its acceptance criteria. The "reported device performance" are the results from the non-clinical testing.

    Acceptance Criteria CategorySpecific Criteria / SpecificationReported Device Performance / Result
    Focal Spot MeasurementLarge focal spot (nominal 0.3 mm): Max dimensions = 0.45mm W x 0.65mm LLarge: 25kV (0.47mm L x 0.33mm W), 28kV (0.46mm L x 0.31mm W), 30kV (0.46mm L x 0.30mm W)
    Small focal spot (nominal 0.1 mm): Max dimensions = 0.15mm W x 0.15mm LSmall: 25kV (0.11mm L x 0.087mm W), 28kV (0.11mm L x = 800 mR/second for at least 3 seconds (through compression paddle at entrance surface of breast)
    Light Field to X-ray Field CongruencyWithin 1% of the SID (0.65 cm) at all edges of the defined x-ray field (21 CFR 2% total)(No specific numerical result provided in the "Results" section, but implicitly met as part of overall performance)
    Light Field IlluminanceMinimum 160 lux (21 CFR, subchapter J. section 1020.31)(No specific numerical result provided in the "Results" section, but implicitly met as part of overall performance)
    Reproducibility (Exposures)Less than 0.05 coefficient of variation for 10 consecutive exposures (as per 21 CFR, internal spec 0.04)(No specific numerical result provided in the "Results" section, but implicitly met as part of overall performance, referenced back to this section from AEC Tracking)
    Linearity (Radiation Output vs. mAs)Less than 0.10 for adjacent mAs selections: (X1-X2)
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