ClearanceBrief
510(k) K873213 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

HICKMAN PLASTIC SUBCUTANEOUS PORT

ApplicantC.R. Bard, Inc., Murray Hill NJ, US
DecisionSubstantially Equivalent, Oct 27, 1987
ReceivedAug 14, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K873213

DateFirm and productCodeLinked 510(k)
Oct 1, 2019Bard Peripheral Vascular Inc
BardPort M.R.I. Implantable Port with Attachale 9.6 F Open-Ended Single-Lumen Venous Catheter, REF: 0602680, UDI:(01)00801741025679 Product Usage: Bard implantable ports are indicated for patient ther
Terminated
LJTNone listed
Oct 1, 2019Bard Peripheral Vascular Inc
BardPort M.R.I. Hard Base Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter, Ref: 0604550, UDI: (01)00801741025860 Product Usage: Bard implantable ports are indicated for
Terminated
LJTNone listed
Mar 1, 2012Bard Access Systems
BardPort M.R.I. Implanted Port with Attachable 6 Fr. ChronoFlex Open-Ended Single-Lumen Venous Catheter and Peel-Apart Introducer Kit. Subcutaneous implanted intravascular infusion port and catheter i
Terminated
LJTNone listed

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