FDA 510(k) Application Details - K140099

Device Classification Name	Catheter, Retention Type, Balloon   More FDA Info for this Device
510(K) Number	K140099
Device Name	Catheter, Retention Type, Balloon
Applicant	SEEDINGS LIFE SCIENCE VENTURES, LLC 230 EAST 15TH STREET SUITE 1-A NEW YORK, NY 10003 US Other 510(k) Applications for this Company
Contact	KEN SOLOVAY Other 510(k) Applications for this Contact
Regulation Number	876.5130   More FDA Info for this Regulation Number
Classification Product Code	EZL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/16/2014
Decision Date	03/04/2014
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