FDA 510(k) Application Details - K971925

Device Classification Name	Catheter, Hemodialysis, Implanted   More FDA Info for this Device
510(K) Number	K971925
Device Name	Catheter, Hemodialysis, Implanted
Applicant	MEDICAL COMPONENTS, INC. 1499 DELP DR. HARLEYSVILLE, PA 19438 US Other 510(k) Applications for this Company
Contact	JEANNE CUSH Other 510(k) Applications for this Contact
Regulation Number	876.5540   More FDA Info for this Regulation Number
Classification Product Code	MSD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/23/1997
Decision Date	02/23/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review