Product code FWL— General, Plastic Surgery
STORZ MODEL 62 ENT CAMERA SYSTEM
- Classification name
- Camera, Cine, Endoscopic, Without Audio
- Device class
- Class 1
- Regulation
- 21 CFR 878.4160
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code FWL
FDA has cleared devices under product code FWL between 1988 and 1995, filed by 2 applicant companies. 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.
Clearances per year
- 1995
- 1988
Top applicants under product code FWL
Recent clearances under product code FWL
Data sourced from openFDA. This site is unofficial and independent of the FDA.