Product code LAW— Clinical Toxicology
BIOTRACK THEOPHYLLINE QUALITY CONTROLS
- Classification name
- Theophylline Control Materials
- Device class
- Class 1
- Regulation
- 21 CFR 862.3280
- Advisory panel
- Clinical Toxicology
- Total cleared
- 4
- First cleared
- Most recent
Market context for product code LAW
FDA has cleared devices under product code LAW between 1987 and 1992, filed by 4 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
- 1992
- 1990
- 1987
Top applicants under product code LAW
Recent clearances under product code LAW
Data sourced from openFDA. This site is unofficial and independent of the FDA.