ClearanceBrief
510(k) K890074 ยท LXJ Interactive Rehabilitation Exercise Devices

SPINETRAK

ApplicantMotion Analysis Corp., Santa Rosa CA, US
DecisionSubstantially Equivalent, Feb 3, 1989
ReceivedJan 9, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890074

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.