Home / 510(k) Clearances / K993496

510(k) K993496

RETIC-QUINOX by Hematronix, Inc. — Product Code JPK

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 30, 1999
Date Received
October 15, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mixture, Hematology Quality Control
Device Class
Class II
Regulation Number
864.8625
Review Panel
HE
Submission Type

Other clearances by Hematronix, Inc.

  • K012243 — MCC URICHECK ASSAYED LIQUID URINE MULTICONSTITUENT CONTROL (August 20, 2001)
  • K972710 — QUANTIFY(901) (August 15, 1997)
  • K960471 — TRI-COUNT 20 (March 20, 1996)
  • K960005 — TRI-COURT 20-T (March 19, 1996)
  • K941965 — EZ-RANGE (April 25, 1995)
  • K935343 — CENTRIFIQ BLOOD CONTROL (January 27, 1994)
  • K904461 — METER TRAX (October 26, 1990)
  • K902389 — TRI-COUNT 16 (August 22, 1990)

Other clearances for product code JPK

  • K160590 — XN CHECK (December 22, 2016)
  • K160586 — XN-L CHECK (December 22, 2016)
  • K160588 — XN CHECK BF (December 22, 2016)
  • K160606 — BC-5D Hematology Control (September 1, 2016)
  • K141964 — XN CHECK (December 5, 2014)
  • K141957 — XN CHECK BF (December 5, 2014)
  • K130962 — R&D 5D RETIC HEMATOLOGY CONTROL (July 24, 2013)
  • K120744 — XN CHECK BF (October 19, 2012)
  • K120742 — XN CHECK (October 19, 2012)
  • K101578 — R&D SYSTEMS BODY FLUID-I HEMATOLOGY CONTROL (April 28, 2011)