Product code LLE— Unknown
BLOOD GAS EXPERSYSTEM 8700
- Classification name
- Stimulator, Spinal-Cord, Implanted For Peripheral Vascular Disease
- Device class
- Class 3
- Advisory panel
- Unknown
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code LLE
FDA has cleared devices under product code LLE between 1983 and 1984, filed by 2 applicant companies. No FDA device recalls reference this product code. Class III devices are high-risk and generally require premarket approval (PMA); 510(k) clearance under a Class III product code is limited to certain preamendments-type devices.
Clearances per year
- 1984
- 1983
Top applicants under product code LLE
Recent clearances under product code LLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.