FDA 510(k) Applications Submitted by LYNNE HAMILTON

FDA 510(k) Number Submission Date Device Name Applicant
K030873 03/20/2003 RANDOX AMMONIA RANDOX LABORATORIES, LTD.
K033278 10/10/2003 RANDOX URIC ACID RANDOX LABORATORIES, LTD.
K023763 11/08/2002 RANDOX FRUCTOSAMINE, FRUCTOSAMINE CALIBRATOR, FRUCTOSAMINE CONTROLS RANDOX LABORATORIES, LTD.
K024014 12/04/2002 RANDOX RX DAYTONA RANDOX LABORATORIES, LTD.


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