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FDA 510(k)

LINDE INTEGRATED VALVE (LIV)

K-Number: K063354 · 2007-04-17

ApplicantLinde Gas Therapeutics
Decision Date2007-04-17
Product CodeECX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LINDE INTEGRATED VALVE (LIV) is the device name listed in this FDA 510(k) record. The listed applicant is Linde Gas Therapeutics. It received FDA 510(k) clearance on 2007-04-17 under 510(k) number K063354. The device is classified under product code ECX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINDE INTEGRATED VALVE (LIV)?

LINDE INTEGRATED VALVE (LIV) is a medical device that received FDA 510(k) clearance on 2007-04-17. The listed applicant is Linde Gas Therapeutics. The 510(k) number is K063354.

When did LINDE INTEGRATED VALVE (LIV) receive FDA 510(k) clearance?

LINDE INTEGRATED VALVE (LIV) received FDA 510(k) clearance on 2007-04-17, under 510(k) number K063354.

Who is the listed applicant for LINDE INTEGRATED VALVE (LIV)?

The FDA 510(k) record lists Linde Gas Therapeutics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LINDE INTEGRATED VALVE (LIV)?

The FDA product code for LINDE INTEGRATED VALVE (LIV) is ECX.

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 Linde Gas Therapeutics 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.

K072926HELONTIX VENT

Related Devices (Code: ECX)

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.

K161179Intelli-OxAir Liquide Healthcare America CorporationK161472Walk-O2-BoutEssex Industries, Inc.K153518Medipure Oxygen-LC SystemPraxair Distribution, Incorporated.K101792LIV LINDE INTERGRATED VALVE-PORTABLE OXYGEN SYSTEM, MODEL M706Linde Gas North America, LLCK062300OX-SOX, MODEL C, D, E,Pattient Safety Innovations, LlpK053117EZ-OX PLUSAir Liquide Healthcare America

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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