510(k) K833862

THAYER MARTIN AGAR by American Biomedical Corp. — Product Code JTY

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 12, 1983
Date Received
November 7, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Culture Media, For Isolation Of Pathogenic Neisseria
Device Class
Class II
Regulation Number
866.2410
Review Panel
MI
Submission Type