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FDA 510(k)

ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER

K-Number: K080360 · 2008-04-08

ApplicantEndologix, Inc.
Decision Date2008-04-08
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Endologix, Inc.. It received FDA 510(k) clearance on 2008-04-08 under 510(k) number K080360. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER?

ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER is a medical device that received FDA 510(k) clearance on 2008-04-08. The listed applicant is Endologix, Inc.. The 510(k) number is K080360.

When did ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER receive FDA 510(k) clearance?

ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER received FDA 510(k) clearance on 2008-04-08, under 510(k) number K080360.

Who is the listed applicant for ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER?

The FDA 510(k) record lists Endologix, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER?

The FDA product code for ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER is DQY.

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 Endologix, Inc. 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.

K120212AFX INTRODUCER SYSTEMK111747ENDOLOGIX AFX INTRODUCER SYSTEMK110090AFX INTRODUCER SYSTEMK991601DUAL LUMEN CATHETER, MODEL DL-35-90

Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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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