510(k) K800310

ORTHO ANTISERA CONTROL by Ortho Diagnostics, Inc. — Product Code KSF

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 5, 1980
Date Received
February 12, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kit, Quality Control For Blood Banking Reagents
Device Class
Class II
Regulation Number
864.9650
Review Panel
HE
Submission Type