ClearanceBrief
510(k) K854461 ยท ILK Transport, Patient, Powered

HANDI-MOVE

ApplicantT.F. Herceg, Inc., New York NY, US
DecisionSubstantially Equivalent, Mar 14, 1986
ReceivedNov 6, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854461

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.