ClearanceBrief
510(k) K973787 ยท MOS Coil, Magnetic Resonance, Specialty

MEDRAD 1.5T EXTREMITY ARRAY

ApplicantMedrad, Inc., Indianola PA, US
DecisionSubstantially Equivalent, Dec 30, 1997
ReceivedOct 6, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K973787

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.