FDA 510(k) Applications Submitted by Kirsten Franco

FDA 510(k) Number	Submission Date	Device Name	Applicant
K191237	05/08/2019	CERENOVUS Large Bore Catheter	Codman & Shurtleff, Inc.
K163357	11/30/2016	OneTouch Via On-Demand Insulin Delivery System	LifeScan Europe, a division of Cilag GmbH
K193380	12/05/2019	CERENOVUS Large Bore Catheter; CERENOVUS Aspiration Tubing Set	Codman & Shurtleff, Inc.
K140227	01/30/2014	MONODERM SURGICAL SUTURE	SURGICAL SPECIALTIES CORP.
K141558	06/12/2014	QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE	SURGICAL SPECIALTIES CORP.
K141778	07/02/2014	QUILL MONODERM KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN	SURGICAL SPECIALTIES CORPORATION