KPH
- Product code
- KPH
- Device name
- Catheter, Rectal For Continent Ileostomy
- Device class
- Class 1
- 21 CFR
- 21 CFR 876.5030
- Medical specialty
- Gastroenterology, Urology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 1 (all years; only the last 3 years are listed here)
Official FDA classification page: KPH
Classification and pathway per current FDA publications. Data from openFDA (CC0).