E.R.C.P.-1 Endoscopic Retrograde Cholangio-Cathete

FDA 510(k) K851964 · Wilson-Cook Medical, Inc.

Substantially Equivalent

510(k) numberK851964

Submission

Device name
E.R.C.P.-1 Endoscopic Retrograde Cholangio-Cathete
Applicant
Wilson-Cook Medical, Inc.
Winston-Salem, NC, US
Received
May 3, 1985
Decision date
June 13, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KNS – Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 876.4300
Specialty
Gastroenterology, Urology

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K252889Single Use 3-Lumen Needle Knife V (KD-V441M, KD-V451M)KNS · Traditional Olympus Medical Systems Corporation11/25/2025SE
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K250351Single Use Electrosurgical Knife (KD-612L, KD-612U); Single Use Electrosurgical Knife…KNS · Traditional Olympus Medical Systems Corporation10/10/2025SE
K251104SureTome™ SW Sphincterotome with DomeTipKNS · Traditional Wilson-Cook Medical09/29/2025SE
K251226Aqua Medical RF Vapor Ablation SystemKNS · Traditional Aqua Medical, Inc.08/08/2025SE
K250584Rezum SystemKNS · Traditional Boston Scientific Corporation06/11/2025SE
K242774SpydrBlade Flex Instrument (PRD-RG1-001)KNS · Traditional Creo Medical, Ltd.06/06/2025SE

More from Creo Medical, Ltd.

510(k)DeviceDecision
K253302Hemospray Endoscopic Hemostat (HEMO-[X])QAU · Traditional 06/02/2026SE
K251104SureTome™ SW Sphincterotome with DomeTipKNS · Traditional 09/29/2025SE
K243568Teslatome Bipolar Sphincterotome; Tesla BiCord Active CordKNS · Special 01/17/2025SE
K213483SnapLoc Wire LockODC · Traditional 04/26/2022SE
K213356Entuit PEG, Entuit PEGJPIF · Special 01/20/2022SESD
K212323Instinct Plus Endoscopic Clipping DevicePKL · Special 08/25/2021SE
K201322Entuit Nasal Jejunal Feeding TubeKNT · Special 06/17/2020SESK
K200972Hemospray Endoscopic HemostatQAU · Traditional 06/10/2020SE
K200247Fusion Quattro Extraction BalloonGCA · Special 02/27/2020SE
K192339TeslaTome Bipolar Sphincterotome, Tesla Bipolar Active CordKNS · Traditional 01/30/2020SE

Questions and answers

When was E.R.C.P.-1 Endoscopic Retrograde Cholangio-Cathete cleared by the FDA?

E.R.C.P.-1 Endoscopic Retrograde Cholangio-Cathete (K851964) received a 510(k) decision of Substantially Equivalent on June 13, 1985, 41 days after the submission was received.

What is the product code of K851964?

The FDA product code is KNS – Unit, Electrosurgical, Endoscopic (With Or Without Accessories), a Class II (moderate risk) device regulated under 21 CFR 876.4300.