KQL — Tube, Tympanostomy With Semi-Permeable Membrane Class II

FDA Device Classification

FDA product code KQL covers "Tube, Tympanostomy With Semi-Permeable Membrane", a Class II medical device regulated under 21 CFR 874.3930. Submissions are reviewed by the Ear, Nose, Throat panel. Devices under this code are implants.

Classification Details

Product Code
KQL
Device Class
Class II
Regulation Number
874.3930
Submission Type
Review Panel
EN
Medical Specialty
Ear, Nose, Throat
Implant
Yes