EXE — Protector, Ostomy Class I

FDA Device Classification

FDA product code EXE covers "Protector, Ostomy", a Class I medical device regulated under 21 CFR 876.5900. Submissions are reviewed by the Gastroenterology, Urology panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
EXE
Device Class
Class I
Regulation Number
876.5900
Submission Type
Review Panel
GU
Medical Specialty
Gastroenterology, Urology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K904233convatec, a division of e.r. squibb and sonsCONVATEC ABSORBENT BANDAGEMarch 6, 1991
K770982howmedicaUNITED SKIN BARRIERJuly 15, 1977
K760927rudolfo t. sanchezSTOMA SHIELD ADAPTERJanuary 26, 1977