510(k) K240926

PeekMed web by Peek Health, S.A. — Product Code LLZ

K240926 is an FDA 510(k) premarket notification submitted by Peek Health, S.A. for the device "PeekMed web". The FDA issued a decision of Substantially Equivalent on Dec 6, 2024. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Peek Health, S.A. has at least 6 other 510(k) clearances on record.