ClearanceBrief
510(k) K053360 ยท CAF Nebulizer (Direct Patient Interface)

AEROLIFE ULTRASONIC NEBULIZER, MODEL P2C

ApplicantAerovectrx Corporation, Carmichael CA, US
DecisionSubstantially Equivalent, Mar 23, 2006
ReceivedDec 2, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K053360

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.