KCI — Trocar, Tracheal Class I

FDA Device Classification

FDA product code KCI covers "Trocar, Tracheal", a Class I medical device regulated under 21 CFR 874.4420. Submissions are reviewed by the Ear, Nose, Throat panel.

Classification Details

Product Code
KCI
Device Class
Class I
Regulation Number
874.4420
Submission Type
Review Panel
EN
Medical Specialty
Ear, Nose, Throat
Implant
No