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FDA 510(k) Application Details - K960739
Device Classification Name
Elevator, Wheelchair
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510(K) Number
K960739
Device Name
Elevator, Wheelchair
Applicant
BARNES,RICHARDSON & COLBURN
1225 EYE STREET, N.W.
WASHINGTON, DC 20005 US
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Contact
ANSIS M HELMANIS
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Regulation Number
890.3930
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Classification Product Code
ING
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More FDA Info for this Product Code
Date Received
02/23/1996
Decision Date
04/01/1996
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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