LIDCORAPID V2 MONITOR— 510(k) K122247

Substantially Equivalent

Lidco, Ltd.

FDA 510(k) clearance K122247 for LIDCORAPID V2 MONITOR, Substantially Equivalent on 2013-03-20. 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: 2012-07-27
Decision date: 2013-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
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.