FDA 510(k) Application Details - K162110

Device Classification Name	Tubes, Gastrointestinal (And Accessories)   More FDA Info for this Device
510(K) Number	K162110
Device Name	Tubes, Gastrointestinal (And Accessories)
Applicant	CORPAK MedSystems, Inc. a Division of Haylard Health 1001 Asbury Dr Buffalo Grove, IL 60089 US Other 510(k) Applications for this Company
Contact	Stephanie Wasielewski Other 510(k) Applications for this Contact
Regulation Number	876.5980   More FDA Info for this Regulation Number
Classification Product Code	KNT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/29/2016
Decision Date	09/15/2016
Decision	SESK - SUBST EQUIV - KIT
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