510(k) K872687

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

K872687 is an FDA 510(k) premarket notification submitted by I.A.F. Production, Inc. for the device "IAFP MUELLER HINTON AGAR W/HEMO. W/CVA ENRICHMENT". The FDA issued a decision of Substantially Equivalent on August 11, 1987. The device falls under product code LKA (Culture Media, Antimicrobial Susceptibility Test), a Class II device regulated under 21 CFR 866.1700. I.A.F. Production, Inc. has at least 10 other 510(k) clearances on record.