LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70— 510(k) K023960

Name: FDA 510(k) clearance K023960
Creator: U.S. Food and Drug Administration
Published: 2003-01-09

Substantially Equivalent

Lidco, Ltd.

FDA 510(k) clearance K023960 for LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70, Substantially Equivalent on 2003-01-09. Applicant: Lidco, Ltd.. Device class: 2.

Clearance details

Applicant: Lidco, Ltd.
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 2002-11-29
Decision date: 2003-01-09
Decision: Substantially Equivalent
Clearance type: Special
Location: London, GB

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.