FDA 510(k) Application Details - K113357

Device Classification Name	More FDA Info for this Device
510(K) Number	K113357
Device Name	POSEY BED
Applicant	J. T. POSEY CO. 5635 PECK RD. ARCADIA, CA 91006 US Other 510(k) Applications for this Company
Contact	BONNIE BISHOP 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	11/14/2011
Decision Date	03/21/2012
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