EPE — Brush, Cleaning, Tracheal Tube Class I

FDA Device Classification

FDA product code EPE covers "Brush, Cleaning, Tracheal Tube", a Class I medical device regulated under 21 CFR 868.5795. Submissions are reviewed by the Anesthesiology panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
EPE
Device Class
Class I
Regulation Number
868.5795
Submission Type
Review Panel
AN
Medical Specialty
Anesthesiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K863635biological and environmental control laboratoriesUPDATED STERILE ENDOTRACHEAL BRUSHESNovember 3, 1986
K862563clinipadTRACHEOSTOMY CLEANSING SOLUTIONJuly 15, 1986