ClearanceBrief
510(k) K040986 ยท LEL Device, Sleep Assessment

CADWELL LIMB MOVEMENT MODULE

ApplicantCadwell Laboratories, Inc., Kennewick WA, US
DecisionSubstantially Equivalent, Jul 1, 2004
ReceivedApr 15, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K040986

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.