ClearanceBrief
510(k) K812166 ยท BYI Percussor, Powered-Electric

PERCUSSOR

ApplicantDhd Medical Products Div. Diemolding Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 18, 1981
ReceivedJul 30, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812166

DateFirm and productCodeLinked 510(k)
Mar 31, 2021Smiths Medical ASD Inc.
Palm Cups - Product Usage: intended to be used to percuss the chest wall to mobilize the secretions within the bronchial tree.
Terminated
BYINone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.