ClearanceBrief
510(k) K915233 ยท DDR Myoglobin, Antigen, Antiserum, Control

MYOGLOBIN RIA TEST KIT

ApplicantPro Diagnostics, Inc., Houston TX, US
DecisionSubstantially Equivalent, Mar 30, 1992
ReceivedNov 22, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915233

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.