ClearanceBrief
510(k) K000935 ยท MOS Coil, Magnetic Resonance, Specialty

KFA-63 KNEE AND FOOT ARRAY

ApplicantMri Devices Corp., Waukesha WI, US
DecisionSubstantially Equivalent, Apr 7, 2000
ReceivedMar 23, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K000935

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.