KBG — Trocar, Sinus Class I

FDA Device Classification

Classification Details

Product Code
KBG
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
K033591clearmedicalREPROCESSED TROCARSJune 3, 2005
K013987adven medicalREPROCESSED DISPOSABLE TROCARSMarch 1, 2002
K844186chesebrough-pond u.s.aCONTINENT STOMA SYSTEM & ACCESSORIESJanuary 15, 1985