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FDA 510(k)

UNITY IS PATIENT VIEWER

K-Number: K020661 · 2002-05-24

ApplicantGeneral Electric Medical Systems Information Techn
Decision Date2002-05-24
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

UNITY IS PATIENT VIEWER 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 2002-05-24 under 510(k) number K020661. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNITY IS PATIENT VIEWER?

UNITY IS PATIENT VIEWER is a medical device that received FDA 510(k) clearance on 2002-05-24. The listed applicant is General Electric Medical Systems Information Techn. The 510(k) number is K020661.

When did UNITY IS PATIENT VIEWER receive FDA 510(k) clearance?

UNITY IS PATIENT VIEWER received FDA 510(k) clearance on 2002-05-24, under 510(k) number K020661.

Who is the listed applicant for UNITY IS PATIENT VIEWER?

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 IS PATIENT VIEWER?

The FDA product code for UNITY IS PATIENT VIEWER is MSX.

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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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