ClearanceBrief
510(k) K101953 ยท CAF Nebulizer (Direct Patient Interface)

SMDIA-1000

ApplicantSouthmedic, Inc., Bonita Springs FL, US
DecisionSubstantially Equivalent, Jan 7, 2011
ReceivedJul 12, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K101953

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.