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FDA 510(k) Applications Submitted by Aicheck Biotech, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K242077
07/16/2024
PocguideTM Multi-Drug Test Cup OTC, PocguideTM Multi-Drug Test Cup
Aicheck Biotech, Inc.
K242498
08/22/2024
Pocguide Multi-Drug Test Panel, Pocguide Multi-Drug Test Panel OTC
Aicheck Biotech, Inc.
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