ClearanceBrief
510(k) K110936 ยท MSD Catheter, Hemodialysis, Implanted

DURAFLOW 2 CHRONIC HEMODIALYSIS CATHETER AND PROCEDURE KIT

ApplicantAngioDynamics, Inc., Latham NY, US
DecisionUnknown, Jun 10, 2011
ReceivedApr 4, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K110936

DateFirm and productCodeLinked 510(k)
May 3, 2024Angiodynamics, Inc.
DURAFLOW 2, 24CM STRAIGHT BASIC KIT -Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012015
Open, Classified
MSDNone listed
May 3, 2024Angiodynamics, Inc.
DURAFLOW 2, 28CM STRAIGHT BASIC KIT, 1 per Bx PG-Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012021
Open, Classified
MSDNone listed
May 3, 2024Angiodynamics, Inc.
DURAFLOW 2, 32CM STRAIGHT BASIC KIT PG-Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012035
Open, Classified
MSDNone listed
May 3, 2024Angiodynamics, Inc.
DURAFLOW 2, 55CM STRAIGHT BASIC KIT PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012115
Open, Classified
MSDNone listed
May 3, 2024Angiodynamics, Inc.
DURAFLOW 2, 24CM STRAIGHT VASC-PAK PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012185
Open, Classified
MSDNone listed
May 3, 2024Angiodynamics, Inc.
DURAFLOW 2, 28CM STRAIGHT VASC-PAK PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012195
Open, Classified
MSDNone listed

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