ClearanceBrief
510(k) K221892 ยท BXQ Rhinoanemometer (Measurement Of Nasal Decongestion)

VISIONAIR

ApplicantPacificmd Biotech, LLC, Henderson NV, US
DecisionSubstantially Equivalent, Oct 5, 2022
ReceivedJun 29, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221892

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.