The record · by panel · 18 panels
The device record by FDA panel
1614 AI-enabled devices on FDA's list, sorted by the 18 advisory panels FDA files them under. Radiology holds most of them; each panel links every device filed under it.
Retrieved from FDA's list, openFDA and MAUDE.
Every panel, with its device count
- Radiology · 40 product codes1230
- Cardiovascular · 49 product codes154
- Neurology · 20 product codes73
- Anesthesiology · 12 product codes30
- Gastroenterology-Urology · 6 product codes27
- Hematology · 4 product codes22
- Ophthalmic · 3 product codes10
- Pathology · 9 product codes10
- Clinical Chemistry · 6 product codes9
- General and Plastic Surgery · 8 product codes9
- Orthopedic · 5 product codes8
- Dental · 5 product codes7
- Microbiology · 5 product codes7
- General Hospital · 3 product codes6
- Clinical Toxcicology · 2 product codes5
- Obstetrics and Gynecology · 3 product codes5
- Ear Nose & Throat · 1 product code1
- Immunology · 1 product code1
The panel is the lead medical specialty FDA assigns to the submission, as FDA’s list states it. It is a filing category, not a statement about where the device is used.
The whole record of FDA AI-enabled medical devices, or what Apodicta does on a medical record.