EXE
- Product code
- EXE
- Device name
- Protector, Ostomy
- Device class
- Class 1
- 21 CFR
- 21 CFR 876.5900
- Medical specialty
- Gastroenterology, Urology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 3
Official FDA classification page: EXE
Classification and pathway per current FDA publications. Data from openFDA (CC0).