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FDA 510(k)

LIDCORAPID V2 MONITOR

K-Number: K122247 · 2013-03-20

ApplicantLidco, Ltd.
Decision Date2013-03-20
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIDCORAPID V2 MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Lidco, Ltd.. It received FDA 510(k) clearance on 2013-03-20 under 510(k) number K122247. 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 LIDCORAPID V2 MONITOR?

LIDCORAPID V2 MONITOR is a medical device that received FDA 510(k) clearance on 2013-03-20. The listed applicant is Lidco, Ltd.. The 510(k) number is K122247.

When did LIDCORAPID V2 MONITOR receive FDA 510(k) clearance?

LIDCORAPID V2 MONITOR received FDA 510(k) clearance on 2013-03-20, under 510(k) number K122247.

Who is the listed applicant for LIDCORAPID V2 MONITOR?

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 LIDCORAPID V2 MONITOR?

The FDA product code for LIDCORAPID V2 MONITOR is DXG.

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Other records listing Lidco, Ltd. as applicant

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Related Devices (Code: DXG)

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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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