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FDA 510(k)

GE OEC EVERVIEW 7500

K-Number: K051490 · 2005-07-07

ApplicantGe Oec Medical Systems, Inc.
Decision Date2005-07-07
Product CodeOXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GE OEC EVERVIEW 7500 is the device name listed in this FDA 510(k) record. The listed applicant is Ge Oec Medical Systems, Inc.. It received FDA 510(k) clearance on 2005-07-07 under 510(k) number K051490. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GE OEC EVERVIEW 7500?

GE OEC EVERVIEW 7500 is a medical device that received FDA 510(k) clearance on 2005-07-07. The listed applicant is Ge Oec Medical Systems, Inc.. The 510(k) number is K051490.

When did GE OEC EVERVIEW 7500 receive FDA 510(k) clearance?

GE OEC EVERVIEW 7500 received FDA 510(k) clearance on 2005-07-07, under 510(k) number K051490.

Who is the listed applicant for GE OEC EVERVIEW 7500?

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

What is the FDA product code for GE OEC EVERVIEW 7500?

The FDA product code for GE OEC EVERVIEW 7500 is OXO.

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Other records listing Ge Oec Medical Systems, Inc. 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.

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Related Devices (Code: OXO)

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.

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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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