Home / 510(k) Clearances / K213917

510(k) K213917

QStat Cartridge by Hemosonics, LLC — Product Code QFR

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 29, 2022
Date Received
December 15, 2021
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Coagulation System For The Measurement Of Whole Blood Viscoelastic Properties
Device Class
Class II
Regulation Number
864.5430
Review Panel
HE
Submission Type

A coagulation system for the measurement of whole blood viscoelastic properties is an in vitro diagnostic device used to evaluate blood coagulation, fibrinolysis, or both, in patients.

Other clearances by Hemosonics, LLC

  • K251404 — Quantra QStat Cartridge (August 25, 2025)
  • K240045 — QStat Cartridge (March 27, 2024)
  • K232215 — Quantra Hemostasis Analyzer (August 24, 2023)
  • K230461 — Quantra Hemostasis Analyzer (March 24, 2023)
  • K223433 — Quantra QPlus System (December 13, 2022)
  • K201513 — Quantra QPlus System (August 21, 2020)
  • DEN180017 — Quantra Hemostasis Analyzer, QPlus Cartridge (March 12, 2019)

Other clearances for product code QFR

  • K251404 — Quantra QStat Cartridge (August 25, 2025)
  • K240045 — QStat Cartridge (March 27, 2024)
  • K232215 — Quantra Hemostasis Analyzer (August 24, 2023)
  • K230461 — Quantra Hemostasis Analyzer (March 24, 2023)
  • K223433 — Quantra QPlus System (December 13, 2022)
  • K201513 — Quantra QPlus System (August 21, 2020)
  • DEN180017 — Quantra Hemostasis Analyzer, QPlus Cartridge (March 12, 2019)