ClearanceBrief
510(k) K021631 ยท MOS Coil, Magnetic Resonance, Specialty

ISA-21 INTERVENTIONAL SPINE ARRAY COIL

ApplicantMri Devices Corp., Waukesha WI, US
DecisionSubstantially Equivalent, Aug 13, 2002
ReceivedMay 17, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K021631

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.