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FDA 510(k) Application Details - K050921
Device Classification Name
Stimulator, Muscle, Powered
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510(K) Number
K050921
Device Name
Stimulator, Muscle, Powered
Applicant
EASYMED INSTRUMENT CO., LTD.
2/F-3/F, NO.2 BEIHAI DA ROAD
LUNJIAO, SHUNDE
GUANGDONG 528303 CN
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Contact
JEFFERY WU
Other 510(k) Applications for this Contact
Regulation Number
890.5850
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Classification Product Code
IPF
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More FDA Info for this Product Code
Date Received
04/13/2005
Decision Date
12/12/2005
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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