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FDA 510(k) Application Details - K183103
Device Classification Name
Stimulator, Muscle, Powered, For Muscle Conditioning
More FDA Info for this Device
510(K) Number
K183103
Device Name
Stimulator, Muscle, Powered, For Muscle Conditioning
Applicant
Dongguan Yingfeng Metal & Plastic Products Co., Ltd
Bianpu District, Lianhu Road, Qiaotou Town
Dongguan 523520 CN
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Contact
Zesheng Chen
Other 510(k) Applications for this Contact
Regulation Number
890.5850
More FDA Info for this Regulation Number
Classification Product Code
NGX
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More FDA Info for this Product Code
Date Received
11/07/2018
Decision Date
09/18/2019
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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