ClearanceBrief
510(k) K253063 ยท BTO Tube, Tracheostomy (W/Wo Connector)

Venti-Trach Tracheostomy Tube (570 Series); Venti-Trach Tracheostomy Tube (571 Series); Venti-Trach Tracheostomy Tube (580 Series); Venti-Trach Tracheostomy Tube (581 Series)

ApplicantVitaltec Corporation, Taichung City, TW
DecisionSubstantially Equivalent, Sep 11, 2026
ReceivedSep 22, 2025
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K253063

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.