ClearanceBrief
510(k) K897046 ยท CBI Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)

LASER RESISTANT TRACHEAL TUBE

ApplicantSheridan Catheter Corp., Argyle NY, US
DecisionSubstantially Equivalent, Mar 23, 1990
ReceivedDec 18, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K897046

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.