Product code LFE— General Hospital
UNICIDE
- Classification name
- Solution, Cold Sterilizing
- Device class
- Class 2
- Regulation
- 21 CFR 880.6885
- Advisory panel
- General Hospital
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code LFE
FDA has cleared device under product code LFE, all in 1983, 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 LFE
Recent clearances under product code LFE
Data sourced from openFDA. This site is unofficial and independent of the FDA.