ClearanceBrief
510(k) K192182 ยท OWB Interventional Fluoroscopic X-Ray System

C015

ApplicantMicronica Srl, Mirandola, IT
DecisionSubstantially Equivalent, Jan 17, 2020
ReceivedAug 12, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192182

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.