FDA 510(k) Applications Submitted by AMDL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K072901 10/11/2007 AMDL-ELISA DR-70 (FDP) IMMUNOASSAY, MODEL DR2101 AMDL, INC.
K981396 04/17/1998 PYLORIPROBE AMDL, INC.


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