ClearanceBrief
510(k) K902193 ยท BTR Tube, Tracheal (W/Wo Connector)

KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP

ApplicantKevtek Medical Products, Inc., Houston TX, US
DecisionSubstantially Equivalent, Mar 15, 1991
ReceivedMay 16, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902193

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.