LLE — Stimulator, Spinal-Cord, Implanted For Peripheral Vascular Disease Class III

FDA Device Classification

FDA product code LLE covers "Stimulator, Spinal-Cord, Implanted For Peripheral Vascular Disease", a Class III medical device. Submissions are reviewed by the Unknown panel. Devices under this code are implants. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

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

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K833430medical intelcomBLOOD GAS EXPERSYSTEM 8700February 10, 1984
K832916critikon companyINIVOX ELECTRODE/CATHETER SYSNovember 14, 1983