ClearanceBrief
510(k) K993307 ยท BZD Ventilator, Non-Continuous (Respirator)

ARIA LX CPAP SYSTEM

ApplicantRespironics, Inc., Murrysville PA, US
DecisionSubstantially Equivalent, Oct 27, 1999
ReceivedOct 4, 1999
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K993307

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.