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FDA 510(k)

LIDCO SYSTEM

K-Number: K962918 · 1999-01-08

ApplicantLidco, Ltd.
Decision Date1999-01-08
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIDCO SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Lidco, Ltd.. It received FDA 510(k) clearance on 1999-01-08 under 510(k) number K962918. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIDCO SYSTEM?

LIDCO SYSTEM is a medical device that received FDA 510(k) clearance on 1999-01-08. The listed applicant is Lidco, Ltd.. The 510(k) number is K962918.

When did LIDCO SYSTEM receive FDA 510(k) clearance?

LIDCO SYSTEM received FDA 510(k) clearance on 1999-01-08, under 510(k) number K962918.

Who is the listed applicant for LIDCO SYSTEM?

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

What is the FDA product code for LIDCO SYSTEM?

The FDA product code for LIDCO SYSTEM is DXG.

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Other records listing Lidco, 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.

K163334LiDCOunity v2 Hemodynamic MonitorK152935LiDCOunity MonitorK131048LIDCO CNAP MODULEK122247LIDCORAPID V2 MONITORK023960LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70K010049PULSECO HEMODYNAMIC MONITOR CM71

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Related Devices (Code: DXG)

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.

K253092Argos Infinity (Rev. 1.0)Retia Medical Systems, Inc.K251275VitalStream ART Connect; VitalStream-HemoCaretaker MedicalK232048Cogent™ Hemodynamic Monitoring System; Cogent™ HMSIcu MedicalK212529Hypotension Decision Assist Model HDA-OR2Directed Systems, Ltd.K192169PulsioFlex Monitoring System with ProAQT SensorPulsion Medical Systems SEK193179EV1000 Clinical PlatformEdwards Lifesciences, LLC

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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