Product code LQA— Radiology
DIGIRAD REUSABLE IMAGE MEDIA
- Classification name
- Media, Reusable Image
- Device class
- Class 1
- Regulation
- 21 CFR 892.1840
- Advisory panel
- Radiology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code LQA
FDA has cleared device under product code LQA, all in 1986, 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 LQA
Recent clearances under product code LQA
Data sourced from openFDA. This site is unofficial and independent of the FDA.