ClearanceBrief
510(k) K912537 ยท BXB Exerciser, Powered

JACE MODEL K200 KNEE CPM DEVICE, MODIFICATION

ApplicantThera Kinetics, Inc., Mt. Laurel NJ, US
DecisionSubstantially Equivalent, Aug 16, 1991
ReceivedJun 10, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912537

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.