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KBT — Punch, Tonsil Class I

FDA Device Classification

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

Classification Details

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