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FDA 510(k) Applications Submitted by Cori Ragan
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180057
01/08/2018
VORTEK URETERAL DOUBLE LOOP STENT
Coloplast Corp
K170362
02/06/2017
VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENTS
Coloplast Corp
K170422
02/13/2017
BIOSOFT DUO DOUBLE LOOP URETERAL STENTS
Coloplast Corp
K180469
02/21/2018
ImaJin Silicone Hydro-Coated Double Loop Ureteral Stent
Coloplast Corp
K170531
02/22/2017
Ureteral Dilators and Percutaneous Nephrostomy Dilators
Coloplast Corp
K171043
04/07/2017
Ureteric Catheters, Flush Ureteric Catheters, Floppy Tip Hydro-Coated Ureteric Catheters
Coloplast Corp
K201007
04/17/2020
In-Ka Ureteral Balloon Dilatation Catheter
Coloplast Corp
K201165
05/01/2020
In-Ka Percutaneous Balloon Dilatation Catheters, Amplatz Sheath
Coloplast Corp
K201436
06/01/2020
Vortek Single Loop Ureteral Stent
Coloplast Corp
K181811
07/06/2018
ReTrace Ureteral Access Sheath
Coloplast A/S
K182122
08/06/2018
Ureteric Catheters
Coloplast Corp
K182831
10/09/2018
SabreLine and SabreGuard Laser Fibers
Coloplast Corp
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