510(k) K872687

IAFP MUELLER HINTON AGAR W/HEMO. W/CVA ENRICHMENT by I.A.F. Production, Inc. — Product Code LKA

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 11, 1987
Date Received
July 7, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Culture Media, Antimicrobial Susceptibility Test
Device Class
Class II
Regulation Number
866.1700
Review Panel
MI
Submission Type