ClearanceBrief
510(k) K821890 ยท BZT Stethoscope, Esophageal, With Electrical Conductors

CRITIKON #817 ESOPHAGEAL MULTI-PROBE

ApplicantCritikon Company, LLC, Mchenry IL, US
DecisionSubstantially Equivalent, Aug 3, 1982
ReceivedJun 25, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821890

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.