ClearanceBrief
510(k) K132764 ยท LEL Device, Sleep Assessment

MOTION WATCH AND PRO-DIARY

ApplicantCamntech, Ltd., Papworth Everard, Cambridgeshire, GB
DecisionSubstantially Equivalent, Jan 21, 2014
ReceivedSep 4, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K132764

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.