JBN — Fibrin Monomer Paracoagulation Class II

FDA Device Classification

FDA product code JBN covers "Fibrin Monomer Paracoagulation", a Class II medical device regulated under 21 CFR 864.7300. Submissions are reviewed by the Hematology panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
JBN
Device Class
Class II
Regulation Number
864.7300
Submission Type
Review Panel
HE
Medical Specialty
Hematology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K854015american bioproductsFS TEST KITMarch 6, 1986
K781814general diagnosticsSULFATE, FIBRIQUIK PROTAMINENovember 8, 1978