KSG

Media, Potentiating For In Vitro Diagnostic Use

Product code: KSG
Device name: Media, Potentiating For In Vitro Diagnostic Use
Device class: Class 2
21 CFR: 21 CFR 864.9600
Medical specialty: Hematology
Marketing pathway: 510(K) Exempt
510(k) clearances (all years, FDA): 13 (all years; only the last 3 years are listed here)

Official FDA classification page: KSG

Classification and pathway per current FDA publications. Data from openFDA (CC0).