ClearanceBrief
510(k) K023686 ยท LNH System, Nuclear Magnetic Resonance Imaging

AURORA MR-GUIDED INTERVENTIONAL SYSTEM

ApplicantAurora Imaging Technology, Inc., North Andover MA, US
DecisionSubstantially Equivalent, Jan 29, 2003
ReceivedNov 1, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023686

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.