1 device · 1 company · 2005

Product code NVI: Diagnostic Software, K-Nearest Neighbor Algorithm, Autoimmune Disease

1 device under product code NVI, 2005, from 1 company. Each record carries FDA's decision, the Indications for Use statement verbatim where the public document carries one (0 of 1 here), the regulation, and MAUDE report counts by product code.

Diagnostic Software, K-Nearest Neighbor Algorithm, Autoimmune Disease. 21 CFR 862.3100, Class II. The device is intended to suggest a systemic autoimmune disease association as an aid for differential diagnosis to be evaluated in conjunction with clinical findings and other laboratory tests. MAUDE held 1 adverse-event report against this product code as of 2026-10-29; reports are unverified and the code is shared by every device of this type.

Retrieved from FDA public records.

Every device, newest decision first

NVI · 1 device
DecisionDeviceCompanyPanelFDA
BIOPLEX 2200 ANA SCREEN WITH MEDICAL DECISION SUK043341 · 510(k)BIO-RAD LABORATORIES, INC.Clinical Toxcicologydatabase entry

Every product code in the record, the whole record of FDA AI-enabled medical devices, or what Apodicta does on a medical record.

Show me on one of my files →

Every device here is authorized for a stated use. See a record read against what it must prove, on your own file.

Show me on my files