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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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