ClearanceBrief
510(k) K230239 ยท HIF Insufflator, Laparoscopic

AirSeal iFS System; AirSeal dV Solution

ApplicantConmed Corporation, Utica NY, US
DecisionSubstantially Equivalent, Sep 20, 2023
ReceivedJan 30, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230239

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.