LKK — Pump, Infusion, Implanted, Programmable Class III

FDA Device Classification

FDA product code LKK covers "Pump, Infusion, Implanted, Programmable", a Class III medical device. Submissions are reviewed by the Unknown panel. Devices under this code are implants.

Classification Details

Product Code
LKK
Device Class
Class III
Regulation Number
Submission Type
Review Panel
HO
Medical Specialty
Unknown
Implant
Yes