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FDA 510(k) Applications Submitted by Acare Technology Co., Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K111617
06/10/2011
PULSE OXIMETER MODEL AB-F1/AH-S1/AH-M1
ACARE TECHNOLOGY CO., LTD.
K182950
10/23/2018
Acare Suction Unit
Acare Technology Co., Ltd.
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