ClearanceBrief
510(k) K993443 ยท ITI Wheelchair, Powered

RTD ARM ASSISTIVE ROBOTIC DEVICE

ApplicantRehabilitation Technologies Division, Fairfield NJ, US
DecisionSubstantially Equivalent, Dec 17, 1999
ReceivedOct 12, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993443

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.