510(k) K133346

SMARTLOG DIABETES MANAGEMENT SOFTWARE by I-Sens, Inc. — Product Code NBW

K133346 is an FDA 510(k) premarket notification submitted by I-Sens, Inc. for the device "SMARTLOG DIABETES MANAGEMENT SOFTWARE". The FDA issued a decision of Substantially Equivalent on December 19, 2013. The device falls under product code NBW (System, Test, Blood Glucose, Over The Counter), a Class II device regulated under 21 CFR 862.1345. I-Sens, Inc. has at least 10 other 510(k) clearances on record.