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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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