Product code IWW— Radiology
ALL-VUE & GAMMA-VUE VIAL SHIELDS
- Classification name
- Shield, Vial
- Device class
- Class 1
- Regulation
- 21 CFR 892.6500
- Advisory panel
- Radiology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code IWW
FDA has cleared device under product code IWW, all in 1993, 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 IWW
Recent clearances under product code IWW
Data sourced from openFDA. This site is unofficial and independent of the FDA.