510(k) K850591

FIAX TOXO-M ANTIBODIES TEST KIT by Intl. Diagnostic Technology — Product Code GLZ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 30, 1985
Date Received
February 14, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antigens, If, Toxoplasma Gondii
Device Class
Class II
Regulation Number
866.3780
Review Panel
MI
Submission Type