KBC — Saw, Nasal Class I

FDA Device Classification

FDA product code KBC covers "Saw, Nasal", a Class I medical device regulated under 21 CFR 874.4420. Submissions are reviewed by the Ear, Nose, Throat panel. At least 4 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
KBC
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
K811887Sierra LaboratoriesSKIN STAPLE EXTRACTORJul 27, 1981
K810187United States Surgical, A Division Of Tyco HealthcAUTO SUTURE PSS SKIN STAPLING INSTRUMENTMar 20, 1981
K810188United States Surgical, A Division Of Tyco HealthcAUTO SUTURE GAS POWERED DISP. LDS STAPLMar 20, 1981
K772379Edward WeckJOSEPH SAWFeb 2, 1978