Home / 510(k) Clearances / K092382

510(k) K092382

NEXUS PRESSURE RATED EXTENSION SETS by Nexus Medical, LLC — Product Code FPA

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 26, 2010
Date Received
August 5, 2009
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Set, Administration, Intravascular
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type

Other clearances by Nexus Medical, LLC

  • K142590 — All Safe Huber Safety Infusion Set (January 16, 2015)
  • K133351 — NEXUS NIS-6P LUER ACTIVATED DEVICE (May 22, 2014)
  • K130879 — NEXUS IV TUBING SET WITH LUER-ACCESSBILE ONE-WAY CHECK VALVE - IV PLUS (July 9, 2013)
  • K130416 — NEXUS TKO-6P LUER ACTIVATED DEVICE (June 12, 2013)
  • K113398 — NEXUS TKO-6, LUER-ACTIVATED DEVICE (April 18, 2012)
  • K092930 — NEXUS INTRAVASCULAR TUBING SETS-PRE-PIERCED (March 10, 2010)
  • K092527 — NEXUS INJECTION SITE, MODEL NIS-8 (February 4, 2010)
  • K081123 — NEXUS I.V. NEEDLESS ACCESS CANNULA FOR INTRAVASCULAR ADMINISTRATION SETS (November 14, 2008)
  • K080976 — NEXUS I.V. FLUID TRANSFER DEVICE (November 10, 2008)
  • K062551 — NEXUS IRRIGATION TUBING SET (December 15, 2006)

Other clearances for product code FPA

  • K251375 — PuraCath Firefly Needleless Connector IT (9005) (February 12, 2026)
  • K251257 — nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Fre (December 4, 2025)
  • K250325 — BD Alaris Pump Infusion Set (October 30, 2025)
  • K251814 — EZ™ IV Administration Set (August 29, 2025)
  • K251854 — SteadiSet infusion set (August 6, 2025)
  • K243841 — Sparta Infusion Set for Insulin (August 1, 2025)
  • K243392 — Infusomat® Space Volumetric Infusion Pump Administration Sets (July 24, 2025)
  • K250616 — Clave™ Neutral-Displacement Needlefree Connectors (June 5, 2025)
  • K242692 — SteadiSet Infusion Set (May 9, 2025)
  • K242763 — JetCan® Pro Safety Huber Needle (May 2, 2025)