ClearanceBrief
510(k) K013592 ยท MOS Coil, Magnetic Resonance, Specialty

EXTREMITY COIL

ApplicantUsa Instruments, Inc., Aurora OH, US
DecisionSubstantially Equivalent, Jan 8, 2002
ReceivedOct 30, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K013592

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.