KAM

Cannula, Sinus

Product code
KAM
Device name
Cannula, Sinus
Device class
Class 1
21 CFR
21 CFR 878.4800
Medical specialty
General, Plastic Surgery
Marketing pathway
510(K) Exempt
510(k) clearances (last 3 years)
19
Official FDA classification page: KAM
Classification and pathway per current FDA publications. Data from openFDA (CC0).