Product code LDX— Pathology
ZINC FORMALIN
- Classification name
- Fixative, Metallic Containing
- Device class
- Class 1
- Regulation
- 21 CFR 864.4010
- Advisory panel
- Pathology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code LDX
FDA has cleared device under product code LDX, 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 LDX
Recent clearances under product code LDX
Data sourced from openFDA. This site is unofficial and independent of the FDA.