FDA 510(k) Application Details - K060944

Device Classification Name	Tube, Feeding   More FDA Info for this Device
510(K) Number	K060944
Device Name	Tube, Feeding
Applicant	VYGON CORP. 2495 GENERAL ARMISTEAD AVE NORRISTOWN, PA 19403 US Other 510(k) Applications for this Company
Contact	COURTNEY SMITH Other 510(k) Applications for this Contact
Regulation Number	876.5980   More FDA Info for this Regulation Number
Classification Product Code	FPD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/06/2006
Decision Date	09/15/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review