ClearanceBrief
510(k) K060842 ยท CAF Nebulizer (Direct Patient Interface)

REVJET TURBO

ApplicantPromedic, Inc., Mccordsville IN, US
DecisionSubstantially Equivalent, Jun 21, 2006
ReceivedMar 28, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060842

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.