Product code LZM— General, Plastic Surgery
AQUAPLAST TIE DOWN DRESSING
- Classification name
- Guard, Skin Graft
- Device class
- Class 1
- Regulation
- 21 CFR 878.4014
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code LZM
FDA has cleared devices under product code LZM between 1989 and 1994, filed by 2 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
- 1994
- 1989
Top applicants under product code LZM
Recent clearances under product code LZM
Data sourced from openFDA. This site is unofficial and independent of the FDA.