FDA 510(k) Application Details - K950967

Device Classification Name	Sleeve, Limb, Compressible   More FDA Info for this Device
510(K) Number	K950967
Device Name	Sleeve, Limb, Compressible
Applicant	V.V.T. HEALTHCARE TECHNOLOGIES, INC. 4122 EAST PONCE DE LEON AVE. SUITE 10 CLARKSTON, GA 30021 US Other 510(k) Applications for this Company
Contact	DEBRA K VANN Other 510(k) Applications for this Contact
Regulation Number	870.5800   More FDA Info for this Regulation Number
Classification Product Code	JOW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/16/1995
Decision Date	05/08/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review