Product code LTD— Unknown
API UNISCEPT MIC
- Classification name
- Paraquat Assay
- Device class
- Class 3
- Advisory panel
- Unknown
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code LTD
FDA has cleared devices under product code LTD between 1984 and 1985, filed by 2 applicant companies. No FDA device recalls reference this product code. Class III devices are high-risk and generally require premarket approval (PMA); 510(k) clearance under a Class III product code is limited to certain preamendments-type devices.
Clearances per year
- 1985
- 1984
Top applicants under product code LTD
Recent clearances under product code LTD
Data sourced from openFDA. This site is unofficial and independent of the FDA.