Product code FEZ— Gastroenterology, Urology
CATHETER, SAMPLING, CONDUIT
- Classification name
- Catheter And Tube, Suprapubic
- Device class
- Class 2
- Regulation
- 21 CFR 876.5090
- Advisory panel
- Gastroenterology, Urology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code FEZ
FDA has cleared device under product code FEZ, all in 1977, filed by 1 applicant company. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Top applicants under product code FEZ
Recent clearances under product code FEZ
Data sourced from openFDA. This site is unofficial and independent of the FDA.