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FDA 510(k) Application Details - K023852
Device Classification Name
Transport, Patient, Powered
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510(K) Number
K023852
Device Name
Transport, Patient, Powered
Applicant
SERVICES INDUSTRIELS SAVARIA, INC.
1225 EYE ST. N.W.
SUITE 1150
WASHINGTON, DC 20005 US
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Contact
ANSIS M HELMANIS
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Regulation Number
890.5150
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Classification Product Code
ILK
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More FDA Info for this Product Code
Date Received
11/19/2002
Decision Date
03/04/2003
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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