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FDA 510(k)

ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK

K-Number: K001972 · 2000-10-27

ApplicantVisicu, Inc.
Decision Date2000-10-27
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK is the device name listed in this FDA 510(k) record. The listed applicant is Visicu, Inc.. It received FDA 510(k) clearance on 2000-10-27 under 510(k) number K001972. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK?

ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK is a medical device that received FDA 510(k) clearance on 2000-10-27. The listed applicant is Visicu, Inc.. The 510(k) number is K001972.

When did ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK receive FDA 510(k) clearance?

ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK received FDA 510(k) clearance on 2000-10-27, under 510(k) number K001972.

Who is the listed applicant for ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK?

The FDA 510(k) record lists Visicu, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK?

The FDA product code for ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK is MSX.

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 Visicu, Inc. 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.

Related Devices (Code: MSX)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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