ClearanceBrief
510(k) K032849 ยท CAF Nebulizer (Direct Patient Interface)

AERONEB GO NEBULIZER, MODEL AG-AG2000

ApplicantAerogen, Inc., Mountain View CA, US
DecisionSubstantially Equivalent, Nov 21, 2003
ReceivedSep 12, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K032849

DateFirm and productCodeLinked 510(k)
Nov 5, 2004Medical Industries America Inc
Aeroneb Go Micropump Nebulizer Featuring OnQ electronic micropump, RX, Manufactured by Medical Industries America Inc., Adel, IA. The product is sold individually or in master packs of 8 under the fo
Terminated
CAFNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.