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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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