FKC — Clamp, Cannula Class I

FDA Device Classification

FDA product code FKC covers "Clamp, Cannula", a Class I medical device regulated under 21 CFR 876.5540. 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
FKC
Device Class
Class I
Regulation Number
876.5540
Submission Type
Review Panel
GU
Medical Specialty
Gastroenterology, Urology
Implant
Yes

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K771419quintonCANNULA CLAMPAugust 26, 1977