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FDA 510(k) Applications Submitted by MEDICORE CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K212412
08/03/2021
IRIS-XP
Medicore Co., Ltd.
K110374
02/09/2011
MAX PULSE SYSTEM
MEDICORE CO., LTD.
K073323
11/27/2007
SA-3000P
MEDICORE CO., LTD.
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