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510(k) K972710

QUANTIFY(901) by Hematronix, Inc. — Product Code JJW

K972710 is an FDA 510(k) premarket notification submitted by Hematronix, Inc. for the device "QUANTIFY(901)". The FDA issued a decision of Substantially Equivalent on August 15, 1997. The device falls under product code JJW (Urinalysis Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Hematronix, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 15, 1997
Date Received
July 21, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Urinalysis Controls (Assayed And Unassayed)
Device Class
Class I
Regulation Number
862.1660
Review Panel
CH
Submission Type

Other clearances by Hematronix, Inc.

  • K012243 — MCC URICHECK ASSAYED LIQUID URINE MULTICONSTITUENT CONTROL (August 20, 2001)
  • K993496 — RETIC-QUINOX (November 30, 1999)
  • 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 JJW

  • K170091 — UA-Cellular Complete (February 9, 2017)
  • K142262 — AUTION CHECK PLUS (April 10, 2015)
  • K131444 — UA-CELLULAR COMPLETE (January 29, 2014)
  • K110846 — RANDOX URINALYSIS CONTROLS, LEVELS 1 AND 2 (September 30, 2011)
  • K103387 — MISSION LIQUID URINE CONTROL, MISSION LIQUID DIPTUBE URINE CONTROL, MISSION DRY (February 2, 2011)
  • K081908 — CLINIQA LIQUID QC URINALYSIS CONTROLS, LEVELS 1 AND 2 (January 16, 2009)
  • K072640 — IRISPEC,CA/CB/CC (December 21, 2007)
  • K070848 — LIQUICHEK URINALYSIS CONTROL (BI-LEVEL), CONTROL LEVEL1, LEVEL 2,MINIPAK, 435,43 (April 25, 2007)
  • K052242 — ADVIA CHEMISTRY MICROALBUMIN CONTROLS (October 3, 2005)
  • K043266 — RANDOX URINE CONTROLS (February 15, 2005)

FDA data resources