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FDA 510(k)

UNITY NETWORK ID

K-Number: K021454 · 2002-10-01

ApplicantGeneral Electric Medical Systems Information Techn
Decision Date2002-10-01
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

UNITY NETWORK ID is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Medical Systems Information Techn. It received FDA 510(k) clearance on 2002-10-01 under 510(k) number K021454. 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 UNITY NETWORK ID?

UNITY NETWORK ID is a medical device that received FDA 510(k) clearance on 2002-10-01. The listed applicant is General Electric Medical Systems Information Techn. The 510(k) number is K021454.

When did UNITY NETWORK ID receive FDA 510(k) clearance?

UNITY NETWORK ID received FDA 510(k) clearance on 2002-10-01, under 510(k) number K021454.

Who is the listed applicant for UNITY NETWORK ID?

The FDA 510(k) record lists General Electric Medical Systems Information Techn as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNITY NETWORK ID?

The FDA product code for UNITY NETWORK ID is MWI.

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Other records listing General Electric Medical Systems Information Techn 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.

K023380T-WAVE ALTERMANS (TWA) ALGORITHM OPTIONK021470SEER LIGHT COMPACT DIGITAL HOLTER RECORDERK023100ACCUSKETCH CARDIAC QUANTITATIVE SYSTEM W/ ADVANCED ANALYSIS COMPONENTSK020290DASH 3000/4000 PATIENT MONITORK021366MAC-LAB/CARDIOLAB EP/COMBOLABK020661UNITY IS PATIENT VIEWER

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Related Devices (Code: MWI)

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.

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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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