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