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FDA 510(k)

GE ADVANTAGE WINDOWS REVIEW WORKSTATION

K-Number: K960613 · 1996-04-30

ApplicantGE Medical Systems
Decision Date1996-04-30
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GE ADVANTAGE WINDOWS REVIEW WORKSTATION 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 1996-04-30 under 510(k) number K960613. 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 GE ADVANTAGE WINDOWS REVIEW WORKSTATION?

GE ADVANTAGE WINDOWS REVIEW WORKSTATION is a medical device that received FDA 510(k) clearance on 1996-04-30. The listed applicant is GE Medical Systems. The 510(k) number is K960613.

When did GE ADVANTAGE WINDOWS REVIEW WORKSTATION receive FDA 510(k) clearance?

GE ADVANTAGE WINDOWS REVIEW WORKSTATION received FDA 510(k) clearance on 1996-04-30, under 510(k) number K960613.

Who is the listed applicant for GE ADVANTAGE WINDOWS REVIEW WORKSTATION?

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 GE ADVANTAGE WINDOWS REVIEW WORKSTATION?

The FDA product code for GE ADVANTAGE WINDOWS REVIEW WORKSTATION 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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