510(k) K855110

DRI-FORM UREAPLASMA DIFFERENTIAL BASAL AGAR MED.A8 by Gibco Laboratories Life Technologies, Inc. — Product Code JSI

K855110 is an FDA 510(k) premarket notification submitted by Gibco Laboratories Life Technologies, Inc. for the device "DRI-FORM UREAPLASMA DIFFERENTIAL BASAL AGAR MED.A8". The FDA issued a decision of Substantially Equivalent on January 7, 1986. The device falls under product code JSI (Culture Media, Selective And Differential), a Class I device regulated under 21 CFR 866.2360. Gibco Laboratories Life Technologies, Inc. has at least 10 other 510(k) clearances on record.