ClearanceBrief
510(k) K994040 ยท MOS Coil, Magnetic Resonance, Specialty

PHASED ARRAY KNEE AND FOOT COIL

ApplicantUsa Instruments, Inc., Aurora OH, US
DecisionSubstantially Equivalent, Jan 18, 2000
ReceivedNov 29, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K994040

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.