KNB — Instrument, Destructive, Fetal, Obstetric Class II

FDA Device Classification

FDA product code KNB covers "Instrument, Destructive, Fetal, Obstetric", a Class II medical device regulated under 21 CFR 884.4500. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
KNB
Device Class
Class II
Regulation Number
884.4500
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K890388kinetic medical productsCEPHALOTOMY SCISSORSFebruary 13, 1989