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FDA 510(k) Applications Submitted by HEMATRONIX, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K960005
01/02/1996
TRI-COURT 20-T
HEMATRONIX, INC.
K960471
02/01/1996
TRI-COUNT 20
HEMATRONIX, INC.
K972710
07/21/1997
QUANTIFY(901)
HEMATRONIX, INC.
K993496
10/15/1999
RETIC-QUINOX
HEMATRONIX, INC.
K012243
07/17/2001
MCC URICHECK ASSAYED LIQUID URINE MULTICONSTITUENT CONTROL
HEMATRONIX, INC.
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