Home / Device Classification / KXG

KXG — Applicator, Absorbent Tipped, Sterile Class I

FDA Device Classification

Classification Details

Product Code
KXG
Device Class
Class I
Regulation Number
880.6025
Submission Type
Review Panel
HO
Medical Specialty
General Hospital
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K802004pollak (intl.)PROFILE SWAB CAT.#5273 & 5274September 16, 1980