ClearanceBrief
510(k) K850320 ยท

NEBULIZER TREATMENT KIT

ApplicantDhd Medical Products Div. Diemolding Corp., Canastota NY, US
DecisionSubstantially Equivalent, Mar 5, 1985
ReceivedJan 28, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850320

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.