510(k) K213737

Quantib ND by Quantib B.V. — Product Code LLZ

K213737 is an FDA 510(k) premarket notification submitted by Quantib B.V. for the device "Quantib ND". The FDA issued a decision of Substantially Equivalent on January 14, 2022. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Quantib B.V. has at least 10 other 510(k) clearances on record.