FDA 510(k) Application Details - K142783

Device Classification Name Wheelchair, Powered

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510(K) Number K142783
Device Name Wheelchair, Powered
Applicant HEARTWAY Medical Products Co., Ltd.
No.6 Road 25, Taichung Industrial Park,
Taichung City 40850 TW
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Contact JEN KE-MIN
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Regulation Number 890.3860

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Classification Product Code ITI
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Date Received 09/26/2014
Decision Date 06/12/2015
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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