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
510(k) Exempt
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,BECKJun 11, 1985
K822524KelleherEAR SPOONSep 9, 1982
K791124XomedSURGICAL SCISSORSJun 27, 1979

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.