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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