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FDA 510(k)

GE 0.7T SIGNA OPENSPEED WITH EXCITE MR SYSTEM

K-Number: K032795 · 2003-10-08

ApplicantGe Medical Systems, LLC
Decision Date2003-10-08
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GE 0.7T SIGNA OPENSPEED WITH EXCITE MR SYSTEM 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 2003-10-08 under 510(k) number K032795. 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 GE 0.7T SIGNA OPENSPEED WITH EXCITE MR SYSTEM?

GE 0.7T SIGNA OPENSPEED WITH EXCITE MR SYSTEM is a medical device that received FDA 510(k) clearance on 2003-10-08. The listed applicant is Ge Medical Systems, LLC. The 510(k) number is K032795.

When did GE 0.7T SIGNA OPENSPEED WITH EXCITE MR SYSTEM receive FDA 510(k) clearance?

GE 0.7T SIGNA OPENSPEED WITH EXCITE MR SYSTEM received FDA 510(k) clearance on 2003-10-08, under 510(k) number K032795.

Who is the listed applicant for GE 0.7T SIGNA OPENSPEED WITH EXCITE MR SYSTEM?

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 GE 0.7T SIGNA OPENSPEED WITH EXCITE MR SYSTEM?

The FDA product code for GE 0.7T SIGNA OPENSPEED WITH EXCITE MR SYSTEM 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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