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FDA 510(k) Application Details - K052375
Device Classification Name
Wheelchair, Standup
More FDA Info for this Device
510(K) Number
K052375
Device Name
Wheelchair, Standup
Applicant
ALILIFE TECHNOLOGICAL CO., LTD.
NO. 58 FU-CHIUN STREET
HSIN CHU CITY 30067 TW
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Contact
Ke-Min Jen
Other 510(k) Applications for this Contact
Regulation Number
890.3900
More FDA Info for this Regulation Number
Classification Product Code
IPL
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More FDA Info for this Product Code
Date Received
08/30/2005
Decision Date
09/09/2005
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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