FDA 510(k) Application Details - K023800

Device Classification Name	Sleeve, Limb, Compressible   More FDA Info for this Device
510(K) Number	K023800
Device Name	Sleeve, Limb, Compressible
Applicant	AIRCAST, INC. 92 RIVER RD. SUMMIT, NJ 07902 US Other 510(k) Applications for this Company
Contact	STEPHEN L KENNEY 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	11/14/2002
Decision Date	02/10/2003
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