KBD — Scissors, Nasal Class I

FDA Device Classification

FDA product code KBD covers "Scissors, Nasal", a Class I medical device regulated under 21 CFR 874.4420. Submissions are reviewed by the Ear, Nose, Throat panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
KBD
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
K851763artiberia13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECKJune 11, 1985
K822524kelleherEAR SPOONSeptember 9, 1982
K791124xomedSURGICAL SCISSORSJune 27, 1979