KST — System, Blood Collection, Vacuum-Assisted, Manual Class I

FDA Device Classification

FDA product code KST covers "System, Blood Collection, Vacuum-Assisted, Manual", a Class I medical device regulated under 21 CFR 864.9125. Submissions are reviewed by the Hematology panel.

Classification Details

Product Code
KST
Device Class
Class I
Regulation Number
864.9125
Submission Type
Review Panel
HE
Medical Specialty
Hematology
Implant
No