ClearanceBrief
510(k) K062689 ยท CAF Nebulizer (Direct Patient Interface)

SIDESTREAM PLUS

ApplicantRespironics , Ltd., Cedar Grove NJ, US
DecisionSubstantially Equivalent, Feb 16, 2007
ReceivedSep 11, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062689

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.