Set, Dialysis, Single Needle With Uni-directional Pump, Reprocessed

Device Code: 2032

Product Code(s): NNG

Device Classification Information

• Device Type ID: 2032
• Device Name: Set, Dialysis, Single Needle With Uni-directional Pump, Reprocessed
• Regulation Description: Hemodialysis System And Accessories.
• Regulation Medical Specialty: Gastroenterology/Urology
• Review Panel: Gastroenterology/Urology
• Premarket Review: Office Of Device Evaluation (ODE); Division Of Reproductive, Gastro-Renal, And Urological Devices (DRGUD); Renal Devices Branch (RNDB)
• Submission Type: 510(k)
• CFR Regulation Number: 876.5820 [🔎]
• FDA Device Classification: Class 2 Medical Device
• Product Code: NNG
• GMP Exempt: No
• Summary MR: Eligible
• Implanted Device: No
• Life Support Device: No
• Third Party Review: Not Third Party Eligible

Recognized Standards

• 9-89 ISO 8638 Third Edition 2010-07-01
  Cadiovascular Implants And Extracorporeal Blood Circuit For Hemodialyzers, Hemodialfilters, And Hemofilters
• 9-98 ISO 13959 Third Edition 2014-04-01
  Water For Haemodialysis And Related Therapies
• 9-99 ISO 23500 Second Edition 2014-04-01
  Guidance For The Preparation And Quality Management Of Fluids For Haemodialysis And Related Therapies
• 9-100 ISO 11663 Second Edition 2014-04-01
  Quality Of Dialysis Fluid For Haemodialysis And Related Therapies

Total Product Life Cycle

• Device Type ID: 2032
• Device: Set, Dialysis, Single Needle With Uni-directional Pump, Reprocessed
• Product Code: NNG
• FDA Device Classification: Class 2 Medical Device
• Regulation Description: Hemodialysis System And Accessories.
• CFR Regulation Number: 876.5820 [🔎]

TPLC Last Update: 2019-04-02 20:04:44