ClearanceBrief
510(k) K223916 ยท KGC Tube, Gastro-Enterostomy

PUMA-G System

ApplicantCoaptech, Inc., Baltimore MD, US
DecisionSubstantially Equivalent, Mar 29, 2023
ReceivedDec 29, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K223916

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.