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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