FDA 510(k) Application Details - K051324

Device Classification Name	Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)   More FDA Info for this Device
510(K) Number	K051324
Device Name	Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)
Applicant	MEDI USA, LP 1800 MASSACHUSETTS AVE., N.W. WASHINGTON, DC 20036-1221 US Other 510(k) Applications for this Company
Contact	GARY L YINGLING Other 510(k) Applications for this Contact
Regulation Number	880.5780   More FDA Info for this Regulation Number
Classification Product Code	DWL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/20/2005
Decision Date	12/05/2005
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