ClearanceBrief
510(k) K850964 ยท BZA Connector, Airway (Extension)

DOUBLE-SWIVEL CONNECTOR

ApplicantSheridan Catheter Corp., Argyle NY, US
DecisionSubstantially Equivalent, May 14, 1985
ReceivedMar 8, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850964

DateFirm and productCodeLinked 510(k)
Sep 16, 2009Teleflex Medical
Hudson RICA Sher-I-Swiv & Sher-I-Swiv F/O, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, for the administration of endobronchial anesth
Terminated
BZANone listed
Sep 16, 2009Teleflex Medical
Hudson RICA Sheridan, ET Tube, Sher-I-Bronch LS, 28FR, 35FR, 37FR, 39FR and 41FR, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, for the
Terminated
BZANone listed
Sep 16, 2009Teleflex Medical
Hudson RICA Sheridan, ET Tube, Sher-I-Bronch RS, 28FR, 35 FR, 37 FR, 39FR and 41 FR, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, for
Terminated
BZANone listed
Sep 16, 2009Teleflex Medical
Hudson RICA Sheridan, Sher-I-Bronch Accessory Pack, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, for the administration of endobronchi
Terminated
BZANone listed
Sep 16, 2009Teleflex Medical
Hudson RICA Sheridan, EB Tube, Sher-I-Bronch, LS, 35FR, Nova Plus, 37FR, 39 FR, and 41 FR, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry
Terminated
BZANone listed

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