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FDA 510(k) Application Details - K964134
Device Classification Name
Elevator, Wheelchair
More FDA Info for this Device
510(K) Number
K964134
Device Name
Elevator, Wheelchair
Applicant
TRUS T LIFT
10808 - 178 ST.
EDMONTON, ALBERTA T5S 1J3 CA
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Contact
RICHARD MEUNIER
Other 510(k) Applications for this Contact
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
10/15/1996
Decision Date
12/31/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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