FDA 510(k) Application Details - K123398

Device Classification Name	Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)   More FDA Info for this Device
510(K) Number	K123398
Device Name	Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)
Applicant	RENFRO CORPORATION 661 LINVILLE ROAD MOUNT AIRY, NC 27030 US Other 510(k) Applications for this Company
Contact	Rebecca K Pine 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	11/05/2012
Decision Date	12/18/2012
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