FLJ — Unit, Airflow, Laminar Class II

FDA Device Classification

FDA product code FLJ covers "Unit, Airflow, Laminar", a Class II medical device regulated under 21 CFR 878.5070. Submissions are reviewed by the General, Plastic Surgery panel.

Classification Details

Product Code
FLJ
Device Class
Class II
Regulation Number
878.5070
Submission Type
Review Panel
HO
Medical Specialty
General, Plastic Surgery
Implant
No