KGG — Tissue Adhesive For Use In Embolization Of Brain Arteriovenous Malformations Class III

FDA Device Classification

FDA product code KGG covers "Tissue Adhesive For Use In Embolization Of Brain Arteriovenous Malformations", a Class III medical device. Submissions are reviewed by the Unknown panel.

Classification Details

Product Code
KGG
Device Class
Class III
Regulation Number
Submission Type
Review Panel
NE
Medical Specialty
Unknown
Implant
No