Nephro-Ureteral Stent

FDA 510(k) K942688 · Uresil Corp.

Substantially Equivalent

510(k) numberK942688

Submission

Device name
Nephro-Ureteral Stent
Applicant
Uresil Corp.
Skokie, IL, US
Received
June 7, 1994
Decision date
June 6, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LJE – Catheter, Nephrostomy
Device class
Unclassified

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K183051Kaye Nephrostomy Tamponade Balloon Catheter and Stent SetLJE · Traditional Cook Incorporated07/16/2019SESK
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K181713Ultraxx Nephrostomy Balloon Catheter SetLJE · Traditional Cook Incorporated08/17/2018SE

More from Cook Incorporated

510(k)DeviceDecision
K093653Uresil Gastrostomy Catheter Kit , Model GCL-630HBKKNT · Traditional 02/23/2010SESK
K053245GP General Purpose Drainage Catheter; Mini-Pig Drainage Catheter; Nephrostomy Catheter…FGE · Special 12/20/2005SE
K041995Modification to: GP General Purpose Drainage Catheter, Mini-Pig Drainage Catheter…GBO · Special 08/19/2004SE
K003753GP General Purpose Drainage Set, Mini-Pigtail Drainage Catheter with Locking Pigtail, GP…FGE · Special 01/04/2001SE
K980278Uresil Vascu-Flo Infusion CatheterDQY · Traditional 11/20/1998SE
K981344Uresil Percutaneous Drainage Catheters with Hydrophilic CoatingLJE · Traditional 09/10/1998SE
K980282Uresil Dilator with Radiopaque MarkerDRE · Traditional 04/24/1998SE
K980889Uresil Nephro-Ureteral StentLJE · Traditional 04/08/1998SE
K972582Uresil GuidewireFGE · Traditional 11/21/1997SE
K972583Uresil General Purpose Drainage Catheter, Uresil Nephrostomy Catheter, Uresil Biliary…FGE · Traditional 08/29/1997SE

Questions and answers

When was Nephro-Ureteral Stent cleared by the FDA?

Nephro-Ureteral Stent (K942688) received a 510(k) decision of Substantially Equivalent on June 6, 1995, 364 days after the submission was received.

What is the product code of K942688?

The FDA product code is LJE – Catheter, Nephrostomy, a Unclassified device.