Product code LXG— Clinical Chemistry
MAGNET PAD
- Classification name
- Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
- Device class
- Class 1
- Regulation
- 21 CFR 862.2050
- Advisory panel
- Clinical Chemistry
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code LXG
FDA has cleared devices under product code LXG between 1989 and 2002, filed by 3 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
- 2002
- 1995
- 1989
Top applicants under product code LXG
Adverse events under product code LXG
product code LXG- Malfunction
- 1,310
- Total
- 1,310
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code LXG
Data sourced from openFDA. This site is unofficial and independent of the FDA.