ClearanceBrief
510(k) K890500 ยท HCC Device, Biofeedback

ELT OR ERGONOMIC LIFT TRAINER

ApplicantPhysical Health Devices, Inc., Pomano Beach FL, US
DecisionSubstantially Equivalent, Jan 3, 1990
ReceivedFeb 1, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890500

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.