KGF — Adhesive, Tissue For Aneurysmorrhaphy Class III

FDA Device Classification

FDA product code KGF covers "Adhesive, Tissue For Aneurysmorrhaphy", a Class III medical device. Submissions are reviewed by the Unknown panel. Devices under this code are implants. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
KGF
Device Class
Class III
Regulation Number
Submission Type
Review Panel
NE
Medical Specialty
Unknown
Implant
Yes

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K890021valleylabSTERILE POLYHESIVE PBS DRESSINGJune 1, 1989