ClearanceBrief
510(k) K963372 ยท FMQ Restraint, Protective

HEELBO ER WRIST RESTRAINT

ApplicantHeelbo, Inc., Libertyville IL, US
DecisionSubstantially Equivalent, Nov 7, 1996
ReceivedAug 27, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963372

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.