FDA 510(k) Applications Submitted by BIOTECX LABORATORIES, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K981824 05/22/1998 OPTICOAT T3 EIA KIT BIOTECX LABORATORIES, INC.
K982298 07/01/1998 OPTICOAT T4 EIA KIT BIOTECX LABORATORIES, INC.


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