ClearanceBrief
510(k) K000002 ยท MOS Coil, Magnetic Resonance, Specialty

MAGNA 5000 PHASED ARRAY CTL SPINE COIL

ApplicantUsa Instruments, Inc., Aurora OH, US
DecisionSubstantially Equivalent, Feb 23, 2000
ReceivedJan 3, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K000002

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.