ClearanceBrief
510(k) K031056 ยท MOS Coil, Magnetic Resonance, Specialty

MODIFICATION TO PREMIER III PHASED ARRAY CTL SPINE COIL

ApplicantUsa Instruments, Inc., Aurora OH, US
DecisionSubstantially Equivalent, May 8, 2003
ReceivedApr 3, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K031056

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.