GHK — Centrifuge, Microsedimentation Class I

FDA Device Classification

FDA product code GHK covers "Centrifuge, Microsedimentation", a Class I medical device regulated under 21 CFR 864.5350. Submissions are reviewed by the Hematology panel.

Classification Details

Product Code
GHK
Device Class
Class I
Regulation Number
864.5350
Submission Type
Review Panel
HE
Medical Specialty
Hematology
Implant
No