1 device · 1 company · 2017

AI-enabled immunology devices on FDA's list

1 device in the Immunology panel, 2017, from 1 company across 1 product code. Each record carries FDA's decision, the Indications for Use statement verbatim where the public document carries one (1 of 1 here), the regulation, and MAUDE report counts by product code.

Retrieved from FDA public records.

Every device, newest decision first

Immunology · 1 device
DecisionDeviceCompanyProduct codeFDA
23andMe Personal Genome ServiceDEN160026 · De Novo23andMe, Inc.PTAdatabase entry

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

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

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