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FDA 510(k)

MODIFICATION TO: UNITY NETWORK ID

K-Number: K071982 · 2007-09-21

ApplicantGe Medical Systems Information Technologies
Decision Date2007-09-21
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO: UNITY NETWORK ID is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems Information Technologies. It received FDA 510(k) clearance on 2007-09-21 under 510(k) number K071982. 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 MODIFICATION TO: UNITY NETWORK ID?

MODIFICATION TO: UNITY NETWORK ID is a medical device that received FDA 510(k) clearance on 2007-09-21. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K071982.

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

MODIFICATION TO: UNITY NETWORK ID received FDA 510(k) clearance on 2007-09-21, under 510(k) number K071982.

Who is the listed applicant for MODIFICATION TO: UNITY NETWORK ID?

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

What is the FDA product code for MODIFICATION TO: UNITY NETWORK ID?

The FDA product code for MODIFICATION TO: UNITY NETWORK ID is MWI.

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Other records listing Ge Medical Systems Information Technologies 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.

K120770QT GUARD PLUS ANALYSIS SYSTEMK102426CARESCAPE MODEL V100 VITAL SIGNS MONITORK09236912SL ECG ANALYSIS PROGRAMK093141MARS HOLTER ANALYSIS WORKSTATIONK092027CARESCAPE MONITOR B850K090702MODIFICATION TO DASH 2500 PATIENT MONITOR

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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.

K260438Vital Signs Monitor (CLEO2)Infinium Medical, Inc.K253417Masimo Root Monitoring SystemMasimo CorporationK253196Midmark 800 Digital Vital Signs Device (1-300-0100, 1-300-0200, 1-300-0300, 1-300-0400)Midmark CorporationK253436c-med0 alphaCosinuss GmbHK250135WAVE Clinical Platform (2.0.000)Baxter Healthcare Corp/ Excel MedicalK241766QMAPP® (Hemo, Hemo Lite, PCM, GO, Hybrid)Fysicon BV

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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