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FDA 510(k) Application Details - K963622
Device Classification Name
Bed, Ac-Powered Adjustable Hospital
More FDA Info for this Device
510(K) Number
K963622
Device Name
Bed, Ac-Powered Adjustable Hospital
Applicant
VAIL PRODUCTS, INC.
235 FIRST ST.
TOLEDO, OH 43605 US
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Contact
NANCY VAIL
Other 510(k) Applications for this Contact
Regulation Number
880.5100
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Classification Product Code
FNL
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More FDA Info for this Product Code
Date Received
09/10/1996
Decision Date
05/07/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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