ClearanceBrief
510(k) K032633 ยท MOS Coil, Magnetic Resonance, Specialty

HRK-63-8 KNEE ARRAY COIL

ApplicantMri Devices Corp., Waukesha WI, US
DecisionSubstantially Equivalent, Sep 25, 2003
ReceivedAug 26, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K032633

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.