KCL — Blower, Powder, Ent Class I

FDA Device Classification

FDA product code KCL covers "Blower, Powder, Ent", a Class I medical device regulated under 21 CFR 874.5220. Submissions are reviewed by the Ear, Nose, Throat panel.

Classification Details

Product Code
KCL
Device Class
Class I
Regulation Number
874.5220
Submission Type
Review Panel
EN
Medical Specialty
Ear, Nose, Throat
Implant
No