Product code EZS— Gastroenterology, Urology
COLOPLAST-DURASEAL OSTOMY APPLIANCE
- Classification name
- Appliance, Colostomy, Disposable
- Device class
- Class 1
- Regulation
- 21 CFR 876.5900
- Advisory panel
- Gastroenterology, Urology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code EZS
FDA has cleared device under product code EZS, all in 1978, 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 EZS
Recent clearances under product code EZS
Data sourced from openFDA. This site is unofficial and independent of the FDA.