ClearanceBrief
510(k) K930741 ยท BTR Tube, Tracheal (W/Wo Connector)

ESOPHAGEAL INTUBATION DETECTOR

ApplicantWolfe-Carney Medical, Salt Lake City UT, US
DecisionSubstantially Equivalent, Aug 7, 1993
ReceivedFeb 12, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930741

DateFirm and productCodeLinked 510(k)
Jul 17, 2012LMA North America Inc
LMA Esophageal Intubation Detector (EID), Catalog Number EID100 The device is used to assist verification of placement of the endotracheal tube or esophageal/tracheal double lumen tube. This device i
Terminated
BTRNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.