DeviceClearance

Product code LWZ— Unknown

KODAK T-MAT C FILM SO-119

Classification name
Tissue Graft Of Less Than 6mm
Device class
Class 3
Advisory panel
Unknown
Total cleared
2
First cleared
Most recent

Market context for product code LWZ

FDA has cleared 2 devices under product code LWZ, all in 1984, 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 LWZ

Recent clearances under product code LWZ

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