Product code FXG— General, Plastic Surgery
3MM DISPOSABLE SPECULA
- Classification name
- Specula Accessories
- Device class
- Class 1
- Regulation
- 21 CFR 878.1800
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code FXG
FDA has cleared device under product code FXG, all in 1989, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Top applicants under product code FXG
Recent clearances under product code FXG
Data sourced from openFDA. This site is unofficial and independent of the FDA.