ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK
K-Number: K001972 · 2000-10-27
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Device Summary
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
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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