ClearanceBrief
510(k) K171899 ยท CBF Chamber, Hyperbaric

Revitalair 430F

ApplicantOxavita Srl, Buenos Aires, AR
DecisionSubstantially Equivalent, Nov 22, 2019
ReceivedJun 26, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K171899

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.