JBR — Test, Heparin Neutralization Class II

FDA Device Classification

FDA product code JBR covers "Test, Heparin Neutralization", a Class II medical device regulated under 21 CFR 864.7525. Submissions are reviewed by the Hematology panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
JBR
Device Class
Class II
Regulation Number
864.7525
Submission Type
Review Panel
HE
Medical Specialty
Hematology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K925452baxter diagnosticsDADE HEPZYMEJanuary 11, 1993
K874373probe-tekPT PRO-CLOTJanuary 5, 1988
K770722bay area hema. onco. clinic. and res. lTHROMBO SCREEN QUANTITATIVE HEPARIN ASSAJuly 11, 1977