ClearanceBrief
510(k) K232544 ยท QTD Endoscopic Suturing Device For Altering Gastric Anatomy For Weight Loss

Apollo ESG NXT System, Apollo REVISE NXT System

ApplicantApollo Endosurgery, Inc., Austin TX, US
DecisionSubstantially Equivalent, Sep 18, 2023
ReceivedAug 22, 2023
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K232544

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.