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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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