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FDA 510(k) Applications Submitted by Jimin Han
FDA 510(k) Number
Submission Date
Device Name
Applicant
K212253
07/19/2021
Apollo Duet (Model : APD-4000)
Weero Co.
K223930
12/30/2022
A1417MCW/A1717MCW/F1417MCW
H&abyz Co., Ltd.
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