ClearanceBrief
510(k) K860105 ยท BTR Tube, Tracheal (W/Wo Connector)

SPIRAL-FLEX

ApplicantSheridan Catheter Corp., Argyle NY, US
DecisionSubstantially Equivalent, Mar 4, 1986
ReceivedJan 13, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860105

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.