(190 days)
The Euro-Diagnostica Immunoscan Anti-GBM Kit is an enzyme immunoassay (EIA) kit for the in vitro diagnostic detection of anti-Glomerular Basement Membrane (GBM) antibodies in human serum. This kit is useful as an aid in the diagnosis of autoimmune renal disorders such as Goodpasture's syndrome.
enzyme immunoassay (EIA) kit
This document is a 510(k) clearance letter for the Immunoscan Anti-GBM Kit, an in vitro diagnostic device. It does not contain the detailed information required to answer the specific questions about acceptance criteria, study design, and performance metrics typically associated with AI/ML device evaluations. The letter primarily confirms that the device is substantially equivalent to a predicate device and can be marketed.
Therefore, I cannot provide the requested information from the provided text. The document does not describe:
- Acceptance criteria or reported device performance
- Sample sizes or data provenance for test sets
- Number or qualifications of experts for ground truth
- Adjudication method
- Multi-reader multi-case (MRMC) comparative effectiveness study or effect size
- Standalone algorithm performance
- Type of ground truth used
- Sample size for the training set
- How ground truth for the training set was established
The document is a regulatory approval notice, not a study report or technical specification for the device's performance.
§ 866.5660 Multiple autoantibodies immunological test system.
(a)
Identification. A multiple autoantibodies immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the autoantibodies (antibodies produced against the body's own tissues) in serum and other body fluids. Measurement of multiple autoantibodies aids in the diagnosis of autoimmune disorders (disease produced when the body's own tissues are injured by autoantibodies).(b)
Classification. Class II (performance standards).