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FDA 510(k)

AW SERVER

K-Number: K081985 · 2008-09-25

ApplicantGe Medical Systems, LLC
Decision Date2008-09-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AW SERVER is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems, LLC. It received FDA 510(k) clearance on 2008-09-25 under 510(k) number K081985. 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 AW SERVER?

AW SERVER is a medical device that received FDA 510(k) clearance on 2008-09-25. The listed applicant is Ge Medical Systems, LLC. The 510(k) number is K081985.

When did AW SERVER receive FDA 510(k) clearance?

AW SERVER received FDA 510(k) clearance on 2008-09-25, under 510(k) number K081985.

Who is the listed applicant for AW SERVER?

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

What is the FDA product code for AW SERVER?

The FDA product code for AW SERVER is LLZ.

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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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