KNE — Set, Anesthesia, Obstetric Class II

FDA Device Classification

FDA product code KNE covers "Set, Anesthesia, Obstetric", a Class II medical device regulated under 21 CFR 884.5100. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
KNE
Device Class
Class II
Regulation Number
884.5100
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K880988bd becton dickinson vacutainer systems preanalyticPUDENDAL/LOCAL ANESTESIA BLOCK TRAYJune 1, 1988
K862358hdcEPICATHJuly 7, 1986