FDA 510(k) Application Details - K020538

Device Classification Name	Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)   More FDA Info for this Device
510(K) Number	K020538
Device Name	Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)
Applicant	BOEHRINGER LABORATORIES 500 E. WASHINGTON ST. NORRISTOWN, PA 19401 US Other 510(k) Applications for this Company
Contact	CHRISTOPHER RADL 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	02/19/2002
Decision Date	05/15/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review