ClearanceBrief
510(k) K953559 ยท BTO Tube, Tracheostomy (W/Wo Connector)

LARKEL DEVICE WITH ATTACHMENTS A-H(MODIFICATION)

ApplicantSeidel Medizin GmbH, Buchendorf, DE
DecisionSubstantially Equivalent, May 16, 1996
ReceivedJun 20, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K953559

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.