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FDA 510(k) Application Details - K113355
Device Classification Name
More FDA Info for this Device
510(K) Number
K113355
Device Name
POSEY BED
Applicant
J. T. POSEY CO.
5635 PECK RD.
ARCADIA, CA 91006 US
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Contact
BONNIE BISHOP
Other 510(k) Applications for this Contact
Regulation Number
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Classification Product Code
OYS
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More FDA Info for this Product Code
Date Received
11/14/2011
Decision Date
05/02/2012
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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