ClearanceBrief
510(k) K983002 ยท CAF Nebulizer (Direct Patient Interface)

MYSTIQUE ULTRASONIC NEBULIZER

ApplicantAirsep Corp., Buffalo NY, US
DecisionSubstantially Equivalent, Oct 16, 1998
ReceivedAug 28, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983002

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.