ClearanceBrief
510(k) K020944 ยท CAF Nebulizer (Direct Patient Interface)

VORTEX VALVED HOLDING CHAMBER

ApplicantPari Innovative Manufacturers, Inc., Midlothian VA, US
DecisionSubstantially Equivalent, May 9, 2002
ReceivedMar 25, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020944

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.