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FDA 510(k) Applications Submitted by Chongqing Kanghua Ruiming S&T Co., Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K171877
06/23/2017
SLM-1ER, SLM-2ER, SLM-3ER
Chongqing Kanghua Ruiming S&T Co., Ltd.
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