FEZ — Catheter And Tube, Suprapubic Class II

FDA Device Classification

FDA product code FEZ covers "Catheter And Tube, Suprapubic", a Class II medical device regulated under 21 CFR 876.5090. Submissions are reviewed by the Gastroenterology, Urology panel. Devices under this code are implants. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
FEZ
Device Class
Class II
Regulation Number
876.5090
Submission Type
Review Panel
GU
Medical Specialty
Gastroenterology, Urology
Implant
Yes

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K771066mentorCATHETER, SAMPLING, CONDUITJuly 11, 1977