FGF — Catheter, Ureteral Disposable (X-Ray) Class II

FDA Device Classification

FDA product code FGF covers "Catheter, Ureteral Disposable (X-Ray)", a Class II medical device regulated under 21 CFR 876.5130. Submissions are reviewed by the Gastroenterology, Urology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
FGF
Device Class
Class II
Regulation Number
876.5130
Submission Type
Review Panel
GU
Medical Specialty
Gastroenterology, Urology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K903994applied urologyURETEROPYELOGRAM CATH FOR RETROGRADE DYE INJECTIONOctober 19, 1990