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FDA 510(k) Applications Submitted by TECO DIAGNOSTICS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160372
02/10/2016
URITEK TC-201 URINE CHEMISTRY TEST SYSTEM
TECO DIAGNOSTICS, INC.
K170200
01/23/2017
Carbon Dioxide Reagent Set
Teco Diagnostics, Inc.
K161527
06/02/2016
Teco Creatinine Enzymatic Reagent Kit
TECO DIAGNOSTICS, INC.
K152835
09/29/2015
URITEK TC-201 URINE CHEMISTRY TEST SYSTEM
TECO DIAGNOSTICS, INC.
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