FDA 510(k) Application Details - K960902

Device Classification Name	Sleeve, Limb, Compressible   More FDA Info for this Device
510(K) Number	K960902
Device Name	Sleeve, Limb, Compressible
Applicant	EUREDUC 5, AVENUE RESIDENCE ANTONT 92160 FR Other 510(k) Applications for this Company
Contact	PHILIPPE P JOUBERT 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	03/05/1996
Decision Date	09/26/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review