ClearanceBrief
510(k) K233020 ยท HIF Insufflator, Laparoscopic

TauTona Pneumoperitoneum Assist Device (TPAD)

ApplicantTautona Group Research & Development, Co., LLC, Redwood City CA, US
DecisionSubstantially Equivalent, Jan 12, 2024
ReceivedSep 22, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233020

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.