Product code FTX— General, Plastic Surgery
REFLECTIVE MIRROR/CO2 LASER SURG CAT. #902002-000
- Classification name
- Mirror, General & Plastic Surgery
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code FTX
FDA has cleared device under product code FTX, all in 1987, 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 FTX
Recent clearances under product code FTX
Data sourced from openFDA. This site is unofficial and independent of the FDA.