KBQ — Knife, Tonsil Class I

FDA Device Classification

FDA product code KBQ covers "Knife, Tonsil", a Class I medical device regulated under 21 CFR 874.4420. Submissions are reviewed by the Ear, Nose, Throat panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

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

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K841005premier dental productsTONSIL KNIFE-VARIOUSMay 30, 1984