FDA 510(k) Applications Submitted by DINDO CARRILLO

FDA 510(k) Number Submission Date Device Name Applicant
K000067 01/10/2000 ALKALINE PHOSPHATASE LIQUID REAGENT-KINETIC, MODELS A504-150 AND A504-500H TECO DIAGNOSTICS
K000102 01/13/2000 GLUCOSE (HEXOKINASE) LIQUID REAGENT, MODEL G518-150 TECO DIAGNOSTICS
K010239 01/25/2001 COCAINE DIPSTICK TEST, MODEL D747-A TECO DIAGNOSTICS
K003987 12/26/2000 URS-1K (KETONE TESST) TECO DIAGNOSTICS


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