Product code LXK— General, Plastic Surgery
MICROSCRAPE
- Classification name
- Scrapper, Skin Specimen
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code LXK
FDA has cleared device under product code LXK, all in 1988, 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 LXK
Recent clearances under product code LXK
Data sourced from openFDA. This site is unofficial and independent of the FDA.