ClearanceBrief
510(k) K031139 ยท MOS Coil, Magnetic Resonance, Specialty

PREMIER III PHASED ARRAY CTL SPINE COIL

ApplicantUsa Instruments, Inc., Aurora OH, US
DecisionSubstantially Equivalent, May 29, 2003
ReceivedApr 10, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031139

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.