FDA 510(k) Application Details - K964103

Device Classification Name	Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)   More FDA Info for this Device
510(K) Number	K964103
Device Name	Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)
Applicant	TOURNIER-BOTTU S.A. 15825 SHADY GROVE RD. ROCKVILLE, MD 20850-3010 US Other 510(k) Applications for this Company
Contact	GEORGE C MURRAY 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	10/11/1996
Decision Date	01/06/1997
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