ClearanceBrief
510(k) K993719 ยท MOS Coil, Magnetic Resonance, Specialty

KAC-300 KNEE ARRAY COIL

ApplicantMri Devices Corp., Waukesha WI, US
DecisionSubstantially Equivalent, Nov 26, 1999
ReceivedNov 3, 1999
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K993719

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.