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510(k) K131814

AMECATH DUAL LUMEN IMPLANTED HEMODIALYSIS CATHETER by Ameco Medical Industries — Product Code MSD

Clearance Details

Decision
SESK (Substantially Equivalent (kit))
Decision Date
July 26, 2013
Date Received
June 20, 2013
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Hemodialysis, Implanted
Device Class
Class II
Regulation Number
876.5540
Review Panel
GU
Submission Type

Other clearances by Ameco Medical Industries

  • K152819 — Amecath Peripheral inserted Central Venous Catheter Sets (February 5, 2016)
  • K131144 — AMECO SHEATH INTRODUCER (August 15, 2013)
  • K123943 — AMECATH DUAL LUMEN HEMODIALYSIS CATHETER (April 2, 2013)
  • K110794 — AMECATH CVC AND AMECATH PRESSURE CVC SHORT TERM SINGLE AND MULTI-LUMEN CATHERIZA (December 21, 2011)
  • K110793 — AMECATH AND AMECATH UNIQATH SOFT SHORT TERM DUAL HEMODIALYSIS CATHETERIZATION KI (December 16, 2011)

Other clearances for product code MSD

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  • K211410 — GlidePath 13F Long-Term Hemodialysis Catheter (June 4, 2021)
  • K203767 — Pristine Long-Term Hemodialysis Catheter (April 2, 2021)
  • K202150 — GlidePath 7.5F Long-Term Dialysis Catheter (November 18, 2020)
  • K202176 — Symetrex LTHD Catheter, Symetrex LTHD Catheter with Sideholes (September 3, 2020)
  • K200627 — GlidePath 10F Long-Term Dialysis Catheter (June 22, 2020)
  • K190527 — GlidePath Long-Term Hemodialysis Catheters, HemoStar Long-Term Hemodialysis Cath (March 5, 2020)
  • K182443 — Pristine Hemodialysis Catheter (May 31, 2019)