FDA 510(k) Application Details - K010068

Device Classification Name	Prosthesis, Esophageal   More FDA Info for this Device
510(K) Number	K010068
Device Name	Prosthesis, Esophageal
Applicant	RUSCH INTL. 50 PLANTATION DR. JAFFERY, NH 03452 US Other 510(k) Applications for this Company
Contact	KARENANN J BROZOWSKI Other 510(k) Applications for this Contact
Regulation Number	878.3610   More FDA Info for this Regulation Number
Classification Product Code	ESW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/08/2001
Decision Date	02/08/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review