Product code LHG— Neurology
EPIDUCER LEAD DELIVERY SYSTEM
- Classification name
- Electrode, Spinal Epidural
- Device class
- Class 2
- Regulation
- 21 CFR 882.5880
- Advisory panel
- Neurology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code LHG
FDA has cleared device under product code LHG, all in 2011, filed by 1 applicant company. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Top applicants under product code LHG
Recent clearances under product code LHG
Data sourced from openFDA. This site is unofficial and independent of the FDA.