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FDA 510(k) Application Details - K103817
Device Classification Name
More FDA Info for this Device
510(K) Number
K103817
Device Name
POSEY BED
Applicant
J. T. POSEY CO.
5635 PECK RD.
ARCADIA, CA 91006 US
Other 510(k) Applications for this Company
Contact
ROBERT KELLEHER
Other 510(k) Applications for this Contact
Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
OYS
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/29/2010
Decision Date
04/22/2011
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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