Home / 510(k) Clearances / K860703

510(k) K860703

U - STAR (MICRO-STAR) by Corning Costar Corp. — Product Code LHI

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 6, 1986
Date Received
February 26, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Set, I.V. Fluid Transfer
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type

Other clearances by Corning Costar Corp.

  • K871559 — CELL LIFTER (May 15, 1987)
  • K823137 — OCTAPETTES (December 3, 1982)
  • K823138 — CELL SCRAPER (November 29, 1982)
  • K803244 — ASSAY STRIPS (February 2, 1981)
  • K803242 — SEROCLUSTER EIA PLATES (January 28, 1981)
  • K803243 — SEROCLUSTER FLEXIBLE VINYL U & V PL. (January 28, 1981)
  • K800240 — SEROCLUSTER U AND V (February 13, 1980)

Other clearances for product code LHI

  • K250345 — Medline Bag Decanter (October 24, 2025)
  • K251715 — FlowArt® Vial Access Device Vented (October 14, 2025)
  • K251676 — Medline Microtek C-Flo Bag Decanter, Sterile (2000S); Medline Microtek Bag Decan (September 16, 2025)
  • K243404 — HyHub™ and HyHub™ Duo Vial Access Devices (July 18, 2025)
  • K240761 — Arisure® Closed Male Luer with Spike Adapter (YM060) (March 21, 2025)
  • K243985 — Rio™ Drug Reconstitution Transfer Device (January 22, 2025)
  • K243486 — SmartSiteTM Vented Vial Access Device (December 6, 2024)
  • K241976 — nextaro® va, 15mm, 5µm (September 6, 2024)
  • K233287 — Vent Vial Adapter (July 26, 2024)
  • K232987 — FlowArt Valve for Vial Access (June 26, 2024)