ClearanceBrief
510(k) K812342 ยท IQF Orthosis, Cervical-Thoracic, Rigid

ZEE EXTRICATION DEVICE

ApplicantZee Medical Products Co., Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 21, 1981
ReceivedAug 18, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812342

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.