510(k) K192727

K-ASSAY (R) RF (Ver.2), K-ASSAY (R) RF Calibrator (Ver.2) by Kamiya Biomedical Company — Product Code DHR

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 20, 2020
Date Received
September 27, 2019
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Rheumatoid Factor
Device Class
Class II
Regulation Number
866.5775
Review Panel
IM
Submission Type