ClearanceBrief
510(k) K837229 ยท

TRANSDUCER MODELS 450, 451, 452, 453, 454

ApplicantHoffrel Instruments, Inc., South Norwalk CT, US
DecisionSubstantially Equivalent, Apr 15, 1983
ReceivedMar 1, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K837229

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.