FDA 510(k) Application Details - K982337

Device Classification Name	Dialyzer, Capillary, Hollow Fiber   More FDA Info for this Device
510(K) Number	K982337
Device Name	Dialyzer, Capillary, Hollow Fiber
Applicant	HAIDYLENA MEDICAL EGYPT 26, MAKRAM EBEID ST. NASR CITY, CAIRO 11371 EG Other 510(k) Applications for this Company
Contact	SAMEH TAMIM Other 510(k) Applications for this Contact
Regulation Number	876.5820   More FDA Info for this Regulation Number
Classification Product Code	FJI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/06/1998
Decision Date	12/29/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review