Surgitek Percutaneous Nephrostomy Cath

FDA 510(k) K830226 · Medical Engineering Corp.

Substantially Equivalent

510(k) numberK830226

Submission

Device name
Surgitek Percutaneous Nephrostomy Cath
Applicant
Medical Engineering Corp.
Walker, MI, US
Received
January 24, 1983
Decision date
February 9, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LJE – Catheter, Nephrostomy
Device class
Unclassified

Other 510(k)s with product code LJE

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K250448Disposable Percutaneous Nephrostomy Dilatation KitLJE · Traditional Shenzhen Trious Medical Technology Co., Ltd.07/03/2025SE
K222705Introducer NeedleLJE · Traditional Youcare Technology Co.,Ltd. (Wuhan)05/22/2023SE
K211911Kolibri Percutaneous Nephrostomy Catheters, Kolibri Percutaneous Nephrostomy Kits…LJE · Traditional Coloplast Corp.03/10/2022SESK
K201165In-Ka Percutaneous Balloon Dilatation Catheters, Amplatz SheathLJE · Traditional Coloplast Corp.12/17/2020SESK
K191498Cook-Cope Loop Nephrostomy Set, Ultrathane Nephrostomy Set with Mac-Loc, Ultrathane…LJE · Traditional Cook Incorporated01/29/2020SESK
K190903Lawson Retrograde Nephrostomy Wire Puncture SetLJE · Traditional Cook Incorporated12/16/2019SE
K183051Kaye Nephrostomy Tamponade Balloon Catheter and Stent SetLJE · Traditional Cook Incorporated07/16/2019SESK
K183035Percutaneous Entry Set, Skinny Needle(R) with Chiba Tip, Disposable Two-part Trocar NeedleLJE · Traditional Cook Incorporated05/17/2019SESK
K181735Percutaneous Neonatal Pigtail Nephrostomy Set, Pediatric Nephrostomy Stent SetLJE · Traditional Cook Incorporated03/27/2019SESK
K181713Ultraxx Nephrostomy Balloon Catheter SetLJE · Traditional Cook Incorporated08/17/2018SE

More from Cook Incorporated

510(k)DeviceDecision
K934141Stand Alone CystometrogramFEN · Traditional 11/18/1993SE
K905289Surgitek(R) Lubri-Flex(Tm) Ureteral StentFAD · Traditional 03/13/1991SE
K903448Surgitek Tex-Span Textured Tissue ExpanderLCJ · Traditional 01/14/1991SE
K902773Surgitek(R) Flexible Ureteroscopy Intro/Sheath SetFGB · Traditional 07/16/1990SE
K884746Surgitek Flat T-SpanLCJ · Traditional 08/10/1989SE
K883274Surgitek (R) Uroflow SystemFFG · Traditional 02/08/1989SE
K881736Surgitek CO2 Delivery SystemFAP · Traditional 08/11/1988SE
K880802Surgitek Articulating Ureteroscope Model SU-11FGB · Traditional 05/26/1988SE
K880801Surgitek Flexible Ureteroscope SU-7 & SU-9FGB · Traditional 05/26/1988SE
K842748Surgitek Reconstruc-Nipple Prosthesis · Traditional 09/26/1984SE

Questions and answers

When was Surgitek Percutaneous Nephrostomy Cath cleared by the FDA?

Surgitek Percutaneous Nephrostomy Cath (K830226) received a 510(k) decision of Substantially Equivalent on February 9, 1983, 16 days after the submission was received.

What is the product code of K830226?

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