FDA 510(k) Application Details - K032387

Device Classification Name	Stripper, Vein, External   More FDA Info for this Device
510(K) Number	K032387
Device Name	Stripper, Vein, External
Applicant	SMITH & NEPHEW, INC. 150 MINUTEMAN RD. ANDOVER, MA 01810 US Other 510(k) Applications for this Company
Contact	KAREN PROVENCHER Other 510(k) Applications for this Contact
Regulation Number	870.4885   More FDA Info for this Regulation Number
Classification Product Code	DWQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/04/2003
Decision Date	10/29/2003
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