FDA 510(k) Applications Submitted by JULIE TAYLOR

FDA 510(k) Number Submission Date Device Name Applicant
K955489 11/27/1995 CALIBRATION SERUM LEVEL 1 & 2 RANDOX LABORATORIES, LTD.
K955797 12/22/1995 IGM IMMUNOTRUBIDIMETRIC & CALIBRATOR RANDOX LABORATORIES, LTD.
K955798 12/22/1995 IGG IMMUNOTURBIDIMETRIC & CALIBRATOR RANDOX LABORATORIES, LTD.


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