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FDA 510(k)

IDEAL SOFTWARE OPTION FOR GE MR SCANNERS

K-Number: K072998 · 2007-11-01

Decision Date2007-11-01
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IDEAL SOFTWARE OPTION FOR GE MR SCANNERS 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 2007-11-01 under 510(k) number K072998. 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 IDEAL SOFTWARE OPTION FOR GE MR SCANNERS?

IDEAL SOFTWARE OPTION FOR GE MR SCANNERS is a medical device that received FDA 510(k) clearance on 2007-11-01. The listed applicant is Ge Medical Systems, LLC. The 510(k) number is K072998.

When did IDEAL SOFTWARE OPTION FOR GE MR SCANNERS receive FDA 510(k) clearance?

IDEAL SOFTWARE OPTION FOR GE MR SCANNERS received FDA 510(k) clearance on 2007-11-01, under 510(k) number K072998.

Who is the listed applicant for IDEAL SOFTWARE OPTION FOR GE MR SCANNERS?

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 IDEAL SOFTWARE OPTION FOR GE MR SCANNERS?

The FDA product code for IDEAL SOFTWARE OPTION FOR GE MR SCANNERS is LNH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Ge Medical Systems, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 92 devices →

Related Devices (Code: LNH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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