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FDA 510(k)

ADVANTAGE V.S. CT/MR RAD DIAGNOSTIC WORKSTATION

K-Number: K913770 · 1991-12-27

ApplicantGeneral Electric Co.
Decision Date1991-12-27
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADVANTAGE V.S. CT/MR RAD DIAGNOSTIC WORKSTATION is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1991-12-27 under 510(k) number K913770. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANTAGE V.S. CT/MR RAD DIAGNOSTIC WORKSTATION?

ADVANTAGE V.S. CT/MR RAD DIAGNOSTIC WORKSTATION is a medical device that received FDA 510(k) clearance on 1991-12-27. The listed applicant is General Electric Co.. The 510(k) number is K913770.

When did ADVANTAGE V.S. CT/MR RAD DIAGNOSTIC WORKSTATION receive FDA 510(k) clearance?

ADVANTAGE V.S. CT/MR RAD DIAGNOSTIC WORKSTATION received FDA 510(k) clearance on 1991-12-27, under 510(k) number K913770.

Who is the listed applicant for ADVANTAGE V.S. CT/MR RAD DIAGNOSTIC WORKSTATION?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADVANTAGE V.S. CT/MR RAD DIAGNOSTIC WORKSTATION?

The FDA product code for ADVANTAGE V.S. CT/MR RAD DIAGNOSTIC WORKSTATION is LNH.

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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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