Product code MRL— General Hospital
SPONGETRAC
- Classification name
- Scale, Sponge, Surgical, Electrically-Powered
- Device class
- Class 1
- Regulation
- 21 CFR 880.2740
- Advisory panel
- General Hospital
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code MRL
FDA has cleared device under product code MRL, all in 1997, 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 MRL
Recent clearances under product code MRL
Data sourced from openFDA. This site is unofficial and independent of the FDA.