ClearanceBrief
510(k) K050299 ยท MOS Coil, Magnetic Resonance, Specialty

HRK-123 KNEE ARRAY COIL

ApplicantMri Devices Corporation, Pewaukee WI, US
DecisionSubstantially Equivalent, Feb 24, 2005
ReceivedFeb 7, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K050299

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.