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FDA 510(k)

PULSECO HEMODYNAMIC MONITOR CM71

K-Number: K010049 · 2001-06-14

ApplicantLidco, Ltd.
Decision Date2001-06-14
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PULSECO HEMODYNAMIC MONITOR CM71 is the device name listed in this FDA 510(k) record. The listed applicant is Lidco, Ltd.. It received FDA 510(k) clearance on 2001-06-14 under 510(k) number K010049. 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 PULSECO HEMODYNAMIC MONITOR CM71?

PULSECO HEMODYNAMIC MONITOR CM71 is a medical device that received FDA 510(k) clearance on 2001-06-14. The listed applicant is Lidco, Ltd.. The 510(k) number is K010049.

When did PULSECO HEMODYNAMIC MONITOR CM71 receive FDA 510(k) clearance?

PULSECO HEMODYNAMIC MONITOR CM71 received FDA 510(k) clearance on 2001-06-14, under 510(k) number K010049.

Who is the listed applicant for PULSECO HEMODYNAMIC MONITOR CM71?

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 PULSECO HEMODYNAMIC MONITOR CM71?

The FDA product code for PULSECO HEMODYNAMIC MONITOR CM71 is DXG.

Related Clinical Trials

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.

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.

View all 7 devices →

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.

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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