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FDA 510(k)

VAS-CATH PERITONEAL DIALYSIS CATHETER

K-Number: K871817 · 1987-07-16

ApplicantVas-Cath of Canada , Ltd.
Decision Date1987-07-16
Product CodeFJS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VAS-CATH PERITONEAL DIALYSIS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Vas-Cath of Canada , Ltd.. It received FDA 510(k) clearance on 1987-07-16 under 510(k) number K871817. The device is classified under product code FJS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAS-CATH PERITONEAL DIALYSIS CATHETER?

VAS-CATH PERITONEAL DIALYSIS CATHETER is a medical device that received FDA 510(k) clearance on 1987-07-16. The listed applicant is Vas-Cath of Canada , Ltd.. The 510(k) number is K871817.

When did VAS-CATH PERITONEAL DIALYSIS CATHETER receive FDA 510(k) clearance?

VAS-CATH PERITONEAL DIALYSIS CATHETER received FDA 510(k) clearance on 1987-07-16, under 510(k) number K871817.

Who is the listed applicant for VAS-CATH PERITONEAL DIALYSIS CATHETER?

The FDA 510(k) record lists Vas-Cath of Canada , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VAS-CATH PERITONEAL DIALYSIS CATHETER?

The FDA product code for VAS-CATH PERITONEAL DIALYSIS CATHETER is FJS.

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 Vas-Cath of Canada , Ltd. 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.

K875188LUER LOCK CONNECTORS / RIDIG P.V.C.K871488VAS-CATH PERMANENT DUAL LUMEN HEMODIALYSIS CATHK871487VAS-CATH PERMANENT SINGLE LUMEN HEMODIALYSIS CATHK863982VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAYK853283VACCESS TM 4006K844854OPTI-FLOW DIGITAL SUBTRACTION ANGIOGRAPHY CAT-KIT

View all 19 devices →

Related Devices (Code: FJS)

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.

K213602Argyle Peritoneal Dialysis Cathetor and Kit, Ritus Peritoneal Dialysis Catheter Tunneling Tool KitCovidien, LLCK180485Argyle Peritoneal Dialysis Catheter and Kits, Argyle Presternal Peritoneal Dialysis Catheter and Kits, Argyle Peritoneal Dialysis Accessory Two Part Titanium Luer Adapter, Argyle Adult Peritoneal Dialysis Accessory Titanium Catheter ExtenderCovidien, LLCK130441FALLER STYLETMedionics International, Inc.K121383PS X SERIES (BASIC COMPONENTS AND CATHETER), PD X SERIES (CATHETER WITH ALL COMPONENTS)Medical Components, Inc.K120130FALLER TROCARMedigroup, Inc.K113354VETA PERITONEAL DIALYSIS CATHETERPfm Medical, Inc.

Official Source

View on FDA Database →

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

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