FDA 510(k) Applications Submitted by JAMES D LAPICOLA

FDA 510(k) Number Submission Date Device Name Applicant
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.


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