DeviceClearance

Product code LXW— Unknown

MOTIONSPECT

Classification name
Column, Adsorption, Low Density, Lipoprotein
Device class
Class 3
Advisory panel
Unknown
Total cleared
1
First cleared
Most recent

Market context for product code LXW

FDA has cleared 1 device under product code LXW, all in 1990, 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 LXW

Recent clearances under product code LXW

Data sourced from openFDA. This site is unofficial and independent of the FDA.