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FDA 510(k)

LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70

K-Number: K023960 · 2003-01-09

ApplicantLidco, Ltd.
Decision Date2003-01-09
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70 is the device name listed in this FDA 510(k) record. The listed applicant is Lidco, Ltd.. It received FDA 510(k) clearance on 2003-01-09 under 510(k) number K023960. 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 LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70?

LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70 is a medical device that received FDA 510(k) clearance on 2003-01-09. The listed applicant is Lidco, Ltd.. The 510(k) number is K023960.

When did LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70 receive FDA 510(k) clearance?

LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70 received FDA 510(k) clearance on 2003-01-09, under 510(k) number K023960.

Who is the listed applicant for LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70?

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 LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70?

The FDA product code for LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70 is DXG.

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Other records listing Lidco, Ltd. as applicant

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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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