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FDA 510(k)

ADVANTAGE WORKSTATION 4.1

K-Number: K020483 · 2002-02-28

ApplicantGE Medical Systems
Decision Date2002-02-28
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADVANTAGE WORKSTATION 4.1 is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems. It received FDA 510(k) clearance on 2002-02-28 under 510(k) number K020483. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANTAGE WORKSTATION 4.1?

ADVANTAGE WORKSTATION 4.1 is a medical device that received FDA 510(k) clearance on 2002-02-28. The listed applicant is GE Medical Systems. The 510(k) number is K020483.

When did ADVANTAGE WORKSTATION 4.1 receive FDA 510(k) clearance?

ADVANTAGE WORKSTATION 4.1 received FDA 510(k) clearance on 2002-02-28, under 510(k) number K020483.

Who is the listed applicant for ADVANTAGE WORKSTATION 4.1?

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

What is the FDA product code for ADVANTAGE WORKSTATION 4.1?

The FDA product code for ADVANTAGE WORKSTATION 4.1 is LLZ.

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Other records listing GE Medical Systems as applicant

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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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