Product code LME— Unknown
THERMAL DIFFUSION CEREBRAL BLOOD FLOW MONITOR
- Classification name
- Monitor, Blood-Flow, Cerebral, Thermal Diffusion
- Device class
- Class 3
- Advisory panel
- Unknown
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code LME
FDA has cleared device under product code LME, all in 1985, filed by 1 applicant company. 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.
Top applicants under product code LME
Recent clearances under product code LME
Data sourced from openFDA. This site is unofficial and independent of the FDA.