ClearanceBrief
510(k) K072136 ยท CAF Nebulizer (Direct Patient Interface)

ULTRASONIC NEBULISER MODEL 2010

ApplicantWilfred Kromker GmbH, Egale WI, US
DecisionSubstantially Equivalent, Jul 15, 2008
ReceivedAug 2, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K072136

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.