Product code KPH— Gastroenterology, Urology
WATERS ILEAL RESERVOIR CATHETER
- Classification name
- Catheter, Rectal For Continent Ileostomy
- Device class
- Class 1
- Regulation
- 21 CFR 876.5030
- Advisory panel
- Gastroenterology, Urology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KPH
FDA has cleared device under product code KPH, all in 1981, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Top applicants under product code KPH
Recent clearances under product code KPH
Data sourced from openFDA. This site is unofficial and independent of the FDA.