ClearanceBrief
510(k) K072670 ยท CAF Nebulizer (Direct Patient Interface)

MODIFICATION TO: EFLOW ELECTRONIC INHALER/NEBULIZER

ApplicantPari Innovative Manufacturers, Inc., Midlothian VA, US
DecisionSubstantially Equivalent, Dec 13, 2007
ReceivedSep 21, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K072670

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.