Modification to: Argus System-Continuous Expert Care Network W/Smart Alrams

FDA 510(k) K012171 · Visicu, Inc.

Substantially Equivalent

510(k) numberK012171

Submission

Device name
Modification to: Argus System-Continuous Expert Care Network W/Smart Alrams
Applicant
Visicu, Inc.
Baltimore, MD, US
Received
July 12, 2001
Decision date
July 24, 2001
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
MSX – System, Network And Communication, Physiological Monitors
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2300
Specialty
Cardiovascular
Life-sustaining
Yes

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K141706Ecare Coordinator (Ecc)DRG · Traditional 09/09/2014SE
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Questions and answers

When was Modification to: Argus System-Continuous Expert Care Network W/Smart Alrams cleared by the FDA?

Modification to: Argus System-Continuous Expert Care Network W/Smart Alrams (K012171) received a 510(k) decision of Substantially Equivalent on July 24, 2001, 12 days after the submission was received.

What is the product code of K012171?

The FDA product code is MSX – System, Network And Communication, Physiological Monitors, a Class II (moderate risk) device regulated under 21 CFR 870.2300.