510(k) K854851

WELLCOGEN N. MENINGITIDIS B/E. COLI K1 ZL24 by Wellcome Diagnostics — Product Code GTJ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 4, 1986
Date Received
December 5, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antisera, All Groups, N. Meningitidis
Device Class
Class II
Regulation Number
866.3390
Review Panel
MI
Submission Type