ClearanceBrief
510(k) K931164 ยท BTR Tube, Tracheal (W/Wo Connector)

RUSCH AGT PVC PREFORM NASAL TRACH TUB/CUF W/MUR EY

ApplicantRusch, Inc., Jeffrey NH, US
DecisionSubstantially Equivalent, Jun 23, 1993
ReceivedMar 8, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K931164

DateFirm and productCodeLinked 510(k)
Jun 29, 2023TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781035
Open, Classified		 BTRNone listed
Jun 29, 2023TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781040
Open, Classified		 BTRNone listed
Jun 29, 2023TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781045
Open, Classified		 BTRNone listed
Jun 29, 2023TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781050
Open, Classified		 BTRNone listed
Jun 29, 2023TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781055
Open, Classified		 BTRNone listed
Jun 29, 2023TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781060
Open, Classified		 BTRNone listed
Jun 29, 2023TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781065
Open, Classified		 BTRNone listed
Jun 29, 2023TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781070
Open, Classified		 BTRNone listed
Jun 29, 2023TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781075
Open, Classified		 BTRNone listed
Jun 29, 2023TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781080
Open, Classified		 BTRNone listed

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