ClearanceBrief
510(k) K801796 ยท FMR Device, Transfer, Patient, Manual

THE COMFORT LIFT

ApplicantGettner Enterprises, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 13, 1980
ReceivedJul 29, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801796

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.