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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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