KAT — Perforator, Antrum Class I

FDA Device Classification

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

Classification Details

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