(69 days)
Agfa's DX-D Imaging Package is indicated for use in general projection radiographic applications to capture for display diagnostic quality radiographic images of human anatomy. The DX-D Imaging Package may be used wherever conventional screen-film systems may be be used.
Agfa's DX-D Imaging Package is not indicated for use in mammography.
Agfa's DX-D Imaging Package is a solid state flat panel x-ray system, a direct radiography (DR) system (product code MQB) intended to capture images of the human body. It is a combination of Agfa's NX workstation and one or more flat-panel detectors.
This submission is to add the DX-D40C/G Flat Panel Detector to Agfa's DX-D Imaging Package portfolio. Agfa's DX-D40C/G is currently marketed by Vieworks as the ViVIX-S Wireless Panel (K122865), which is one of predicates for this submission.
Principles of operation and technological characteristics of the new and predicate devices are the same. The new device is physically and electronically identical to both predicates, K121095 and K122865. It uses the same workstation as predicate K121095 and the same scintillatorphotodetector flat panel detectors to capture and digitize the images as predicate K122865.
I am sorry but I can't fulfill your request. The document describes that the new device, Agfa's DX-D Imaging Package, is substantially equivalent to two predicate devices (K121095 and K122865) and does not provide explicit acceptance criteria with specific numerical thresholds for performance metrics. This makes it difficult to directly populate the "Acceptance Criteria" column of the table you requested with quantitative values. Also, the document states "image quality clinical evaluations" were done but lacks the details of such a study. Without additional information, I am unable to describe the acceptance criteria and study as requested.
§ 892.1680 Stationary x-ray system.
(a)
Identification. A stationary x-ray system is a permanently installed diagnostic system intended to generate and control x-rays for examination of various anatomical regions. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.(b)
Classification. Class II (special controls). A radiographic contrast tray or radiology diagnostic kit intended for use with a stationary x-ray system only is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 892.9.