FDA 510(k) Application Details - K955270

Device Classification Name	Clamp, Vascular   More FDA Info for this Device
510(K) Number	K955270
Device Name	Clamp, Vascular
Applicant	ROBERT R. STEVENS 15720 BULL RUN RD. #377 MIAMI LAKES, FL 33014 US Other 510(k) Applications for this Company
Contact	MARIAN D HARDING Other 510(k) Applications for this Contact
Regulation Number	870.4450   More FDA Info for this Regulation Number
Classification Product Code	DXC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/15/1995
Decision Date	08/08/1996
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