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FDA 510(k) Applications Submitted by KIRSTEN STOWELL 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
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