ClearanceBrief
510(k) K032121 ยท LNH System, Nuclear Magnetic Resonance Imaging

MODIFICATION TO E-SCAN XQ

ApplicantEsaote, S.p.A., Indianpolis IN, US
DecisionSubstantially Equivalent, Aug 13, 2003
ReceivedJul 9, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K032121

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.