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FDA 510(k)

WALLSTENT BILIARY ENDOPROTHESES

K-Number: K923993 · 1994-09-30

ApplicantSchneider U.S. Stent Div.
Decision Date1994-09-30
Product CodeFGE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WALLSTENT BILIARY ENDOPROTHESES is the device name listed in this FDA 510(k) record. The listed applicant is Schneider U.S. Stent Div.. It received FDA 510(k) clearance on 1994-09-30 under 510(k) number K923993. The device is classified under product code FGE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WALLSTENT BILIARY ENDOPROTHESES?

WALLSTENT BILIARY ENDOPROTHESES is a medical device that received FDA 510(k) clearance on 1994-09-30. The listed applicant is Schneider U.S. Stent Div.. The 510(k) number is K923993.

When did WALLSTENT BILIARY ENDOPROTHESES receive FDA 510(k) clearance?

WALLSTENT BILIARY ENDOPROTHESES received FDA 510(k) clearance on 1994-09-30, under 510(k) number K923993.

Who is the listed applicant for WALLSTENT BILIARY ENDOPROTHESES?

The FDA 510(k) record lists Schneider U.S. Stent Div. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WALLSTENT BILIARY ENDOPROTHESES?

The FDA product code for WALLSTENT BILIARY ENDOPROTHESES is FGE.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Schneider U.S. Stent Div. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K923119WALLSTENT ESOPHAGEAL PROTHESISK914277WALLSTENT(R) TRANS BILIARY ENDO W/UNISTEP DELIV SY

Related Devices (Code: FGE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254179Drainage CatheterCanyon Medical, Inc.K262913Protégé™ EverFlex™ Self-expanding Peripheral Stent SystemMedtronic, Inc.K260835ARCHIMEDES Biodegradable Stent (Medium)Q3 Medical USA, LLC (C/O Q3 Medical Devices Ltd.)K253393Single-use Balloon Dilatation Catheter (AG-5251-083018 AG-5251-085518 AG-5251-088018 AG-5251-083019 AG-5251-085519 AG-5251-088019 AG-5251-083021 AG-5251-085521 AG-5251-088021 AG-5251-083024 AG-5251-085524 AG-5251-088024 AG-5251-103018 AG-5251-105518 AG-5251-108018 AG-5251-103019 AG-5251-105519 AG-5251-108019 AG-5251-103021 AG-5251-105521 AG-5251-108021 AG-5251-103024 AG-5251-105524 AG-5251-108024 AG-5251-123018 AG-5251-125518 AG-5251-128018 AG-5251-123019 AG-5251-125519 AG-5251-128019Hangzhou AGS MedTech Co., Ltd.K253832Dilation Balloon CatheterMirco-Tech (Nanjing) Co., Ltd.K251658Endoflux™ Biliary & Pancreatic Stent SetsMedi-Globe GmbH

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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