FGY — Cannula, Injection Class I

FDA Device Classification

FDA product code FGY covers "Cannula, Injection", a Class I medical device regulated under 21 CFR 878.4200. Submissions are reviewed by the General, Plastic Surgery panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
FGY
Device Class
Class I
Regulation Number
878.4200
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K822201kelleherEAR CANNULASOctober 6, 1982
K760389b. braun instrumentsCANNULA, IVNovember 2, 1976