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FDA 510(k)

CENTRA VIEW DEVICE LINK SYSTEM

K-Number: K033283 · 2003-10-27

ApplicantIcu Datasystems, Inc.
Decision Date2003-10-27
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTRA VIEW DEVICE LINK SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Icu Datasystems, Inc.. It received FDA 510(k) clearance on 2003-10-27 under 510(k) number K033283. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRA VIEW DEVICE LINK SYSTEM?

CENTRA VIEW DEVICE LINK SYSTEM is a medical device that received FDA 510(k) clearance on 2003-10-27. The listed applicant is Icu Datasystems, Inc.. The 510(k) number is K033283.

When did CENTRA VIEW DEVICE LINK SYSTEM receive FDA 510(k) clearance?

CENTRA VIEW DEVICE LINK SYSTEM received FDA 510(k) clearance on 2003-10-27, under 510(k) number K033283.

Who is the listed applicant for CENTRA VIEW DEVICE LINK SYSTEM?

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

What is the FDA product code for CENTRA VIEW DEVICE LINK SYSTEM?

The FDA product code for CENTRA VIEW DEVICE LINK SYSTEM is MWI.

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Related Devices (Code: MWI)

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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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