ClearanceBrief
510(k) K920755 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

L-CATH PEEL AWAY SYSTEM CATHETER

ApplicantLuther Medical Products, Inc., Tustin CA, US
DecisionSubstantially Equivalent, Jun 7, 1993
ReceivedFeb 19, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920755

DateFirm and productCodeLinked 510(k)
Dec 15, 2005Becton Dickinson Medical Systems
16 G / 5F Dual Lumen L-Cath catheter only.
Terminated
LJSNone listed
Dec 15, 2005Becton Dickinson Medical Systems
16 G / 5F Dual Lumen L-Cath Basic Kit with Insyte Autoguard
Terminated
LJSNone listed
Dec 15, 2005Becton Dickinson Medical Systems
16 G / 5F Dual Lumen L-Cath Complete Kit with Introsyte Autoguard
Terminated
LJSNone listed
Dec 15, 2005Becton Dickinson Medical Systems
16 G / 5F Dual Lumen L-Cath Basic Kit with Introsyte
Terminated
LJSNone listed
Dec 15, 2005Becton Dickinson Medical Systems
16 G / 5F Dual Lumen L-Cath Complete Kit with Introsyte
Terminated
LJSNone listed
Dec 15, 2005Becton Dickinson Medical Systems
16 G / 5F Dual Lumen L-Cath Basic Kit with U-Wing
Terminated
LJSNone listed
Dec 15, 2005Becton Dickinson Medical Systems
16 G / 5F Dual Lumen L-Cath complete kit with U-Wing
Terminated
LJSNone listed
Jul 20, 2004Becton Dickinson Infusion Therapy
BD L-Cath NN (24ga x 30cm), L-Cath Catheter System
Terminated
LJSNone listed
Jul 20, 2004Becton Dickinson Infusion Therapy
BD L-Cath EX (20ga x 15cm), L-Cath Catheter System
Terminated
LJSNone listed
Jul 20, 2004Becton Dickinson Infusion Therapy
BD L-Cath EX (28ga x 20cm), L-Cath Catheter System
Terminated
LJSNone listed

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